def test_context_and_annotations():
braf_no_act = Agent('BRAF', db_refs={'HGNC': '1097', 'UP': 'P15056'})
mek = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'})
ev = Evidence(source_api='reach',
annotations={'string_val': 'x',
'int_val': 5,
'dict_val': {'x': 5},
'list_val': ['a', 'b']},
context=BioContext(
cell_type=RefContext('HCC366',
db_refs={'EFO': '0003131'})))
stmt = Activation(braf_no_act, mek, evidence=[ev])
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
_, _, data = list(belgraph.edges(data=True))[0]
assert data['annotations']['cell_type'] == {'EFO:0003131': True}
assert 'string_val' not in data['annotations']
pba = pa.PybelAssembler([stmt], annotations_to_include=['string_val',
'int_val',
'dict_val',
'list_val'])
belgraph = pba.make_model()
_, _, data = list(belgraph.edges(data=True))[0]
assert data['annotations']['cell_type'] == {'EFO:0003131': True}
assert data['annotations']['string_val'] == {'x': True}
assert data['annotations']['int_val'] == {5: True}
assert 'dict_val' not in data['annotations']
assert data['annotations']['list_val'] == {'a': True, 'b': True}
def test_autophosphorylation():
egfr = Agent('EGFR', db_refs={'HGNC': id('EGFR')})
stmt = Autophosphorylation(egfr, 'Y', '1173')
stmt_hash = stmt.get_hash(refresh=True)
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert len(belgraph) == 2
assert egfr_dsl in belgraph
egfr_phos_node = egfr_dsl.with_variants(egfr_phos_dsl)
assert egfr_dsl in belgraph
assert egfr_phos_node in belgraph
assert belgraph.number_of_nodes() == 2
assert belgraph.number_of_edges() == 2
# There will be two edges between these nodes
edge_dicts = list(belgraph.get_edge_data(egfr_dsl,
egfr_phos_node).values())
assert {pc.RELATION: pc.DIRECTLY_INCREASES,
pc.ANNOTATIONS: {
'stmt_hash': {stmt_hash: True},
'uuid': {stmt.uuid: True},
'belief': {stmt.belief: True},
}} in edge_dicts
# Test an autophosphorylation with a bound condition
tab1 = Agent('TAB1', db_refs={'HGNC': id('TAB1')})
p38_tab1 = Agent('MAPK14', bound_conditions=[BoundCondition(tab1)],
db_refs={'HGNC': id('MAPK14')})
stmt = Autophosphorylation(p38_tab1, 'Y', '100')
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert belgraph.number_of_nodes() == 4
assert belgraph.number_of_edges() == 4
def test_gef():
gef = Agent('SOS1',
mods=[ModCondition('phosphorylation')],
db_refs={'HGNC': '11187'})
ras = Agent('KRAS', db_refs={'HGNC': '6407'})
stmt = Gef(gef, ras)
stmt_hash = stmt.get_hash(refresh=True)
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert len(belgraph) == 3
assert belgraph.number_of_edges() == 2
gef_reference_node = protein(namespace='HGNC',
name='SOS1',
identifier='11187')
gef_node = gef_reference_node.with_variants(pmod('Ph'))
assert gef_reference_node in belgraph
assert gef_node in belgraph
assert kras_node in belgraph
edge_data = get_edge_data(belgraph, gef_node, kras_node)
edge = {
pc.RELATION: pc.DIRECTLY_INCREASES,
pc.SUBJECT: activity('gef'),
pc.OBJECT: activity('gtp'),
pc.ANNOTATIONS: {
'stmt_hash': stmt_hash,
'uuid': stmt.uuid,
'belief': stmt.belief,
},
}
assert edge_data == edge, edge_data
def test_modification_with_evidences():
braf_kin = Agent('BRAF', activity=ActivityCondition('kinase', True),
db_refs={'HGNC': '1097', 'UP': 'P15056'})
mek = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'})
evidence = Evidence(source_api='test', text='evidence text', pmid='1234', epistemics={
'dummy': ['a', 'b'],
'scalar': 'yes',
'missing': None,
})
stmt = Phosphorylation(braf_kin, mek, 'S', '218', evidence=evidence)
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert belgraph.number_of_nodes() == 3, belgraph.number_of_nodes()
assert braf_dsl in belgraph
map2k1_mod_dsl = map2k1_dsl.with_variants(phos_dsl)
assert map2k1_mod_dsl in belgraph
assert belgraph.number_of_edges() == 2
edge_data = get_edge_data(belgraph, braf_dsl, map2k1_mod_dsl)
assert edge_data.get(pc.SUBJECT) == activity('kin')
assert edge_data[pc.RELATION] == pc.INCREASES
assert edge_data.get(pc.EVIDENCE) == 'evidence text', edge_data
assert edge_data[pc.CITATION] == {
pc.CITATION_DB: pc.CITATION_TYPE_PUBMED,
pc.CITATION_IDENTIFIER: '1234',
}
assert 'source_api' in edge_data[pc.ANNOTATIONS]
assert 'test' in edge_data[pc.ANNOTATIONS]['source_api']
assert 'source_id' not in edge_data[pc.ANNOTATIONS]
assert 'source_hash' in edge_data[pc.ANNOTATIONS]
assert 'dummy' in edge_data[pc.ANNOTATIONS]
assert 'a' in edge_data[pc.ANNOTATIONS]['dummy']
assert 'b' in edge_data[pc.ANNOTATIONS]['dummy']
assert 'scalar' in edge_data[pc.ANNOTATIONS]
assert 'yes' in edge_data[pc.ANNOTATIONS]['scalar']
assert 'missing' not in edge_data[pc.ANNOTATIONS]
def test_gap():
gap = Agent('RASA1', mods=[ModCondition('phosphorylation')],
db_refs={'HGNC': '9871'})
ras = Agent('KRAS', db_refs={'HGNC': '6407'})
stmt = Gap(gap, ras)
stmt_hash = stmt.get_hash(refresh=True)
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert len(belgraph) == 3
assert belgraph.number_of_edges() == 2
gap_reference_node = protein(
namespace='HGNC', name='RASA1', identifier='9871')
gap_node = gap_reference_node.with_variants(pmod('Ph'))
ras_node = protein(namespace='HGNC', name='KRAS', identifier='6407')
assert gap_reference_node in belgraph
assert gap_node in belgraph
assert ras_node in belgraph
edge_data = get_edge_data(belgraph, gap_node, ras_node)
edge = {
pc.RELATION: pc.DIRECTLY_DECREASES,
pc.SUBJECT: activity('gap'),
pc.OBJECT: activity('gtp'),
pc.ANNOTATIONS: {
'stmt_hash': {stmt_hash: True},
'uuid': {stmt.uuid: True},
'belief': {stmt.belief: True},
},
}
assert edge_data == edge, edge_data
def test_activation():
braf_no_act = Agent('BRAF', db_refs={'HGNC': '1097', 'UP': 'P15056'})
braf_kin = Agent('BRAF', activity=ActivityCondition('kinase', True),
db_refs={'HGNC': '1097', 'UP': 'P15056'})
mek = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'})
stmt1 = Activation(braf_no_act, mek)
stmt2 = Activation(braf_kin, mek, 'kinase')
edge1 = {
pc.RELATION: pc.INCREASES,
pc.OBJECT: {pc.MODIFIER: pc.ACTIVITY}
}
edge2 = {
pc.RELATION: pc.INCREASES,
pc.SUBJECT: activity('kin'),
pc.OBJECT: activity('kin')
}
for stmt, edge in ((stmt1, edge1), (stmt2, edge2)):
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert len(belgraph.nodes()) == 2
assert braf_dsl in belgraph
assert map2k1_dsl in belgraph
assert belgraph.number_of_edges() == 1
edge_data = get_first_edge_data(belgraph)
assert edge_data == edge
def test_complex_with_complex():
grb2 = Agent('GRB2', db_refs={'HGNC': id('GRB2')})
egfr_grb2 = Agent('EGFR', db_refs={'HGNC': id('EGFR')},
bound_conditions=[BoundCondition(grb2)])
sos1_phos = Agent('SOS1',
mods=[ModCondition('phosphorylation', 'Y', '100')],
db_refs={'HGNC': id('SOS1')})
stmt = Complex([sos1_phos, egfr_grb2])
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert len(belgraph) == 6
assert belgraph.number_of_edges() == 5
egfr_grb2_complex = complex_abundance([egfr_dsl, grb2_dsl])
egfr_grb2_complex_sos1_phos_complex = complex_abundance([
egfr_grb2_complex,
sos1_dsl.with_variants(pmod('Ph', 'Tyr', 100))
])
assert egfr_grb2_complex in belgraph
for member in egfr_grb2_complex.members:
assert member in belgraph
assert egfr_grb2_complex_sos1_phos_complex in belgraph
for member in egfr_grb2_complex_sos1_phos_complex.members:
assert member in belgraph
def test_belgraph_to_signed_graph():
braf_no_act = Agent('BRAF', db_refs={'HGNC': '1097', 'UP': 'P15056'})
mek = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'})
stmt = Activation(braf_no_act, mek)
hsh = stmt.get_hash(refresh=True)
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
pb_seg = pa.belgraph_to_signed_graph(belgraph, propagate_annotations=True)
assert len(pb_seg.edges) == 1
edge = (braf_dsl, map2k1_dsl, 0)
assert edge in pb_seg.edges
edge_dict = pb_seg.edges.get(edge)
assert edge_dict
assert 'stmt_hash' in edge_dict
assert isinstance(edge_dict['stmt_hash'], int)
assert hsh == edge_dict['stmt_hash']
assert 'uuid' in edge_dict
assert isinstance(edge_dict['uuid'], str)
assert stmt.uuid == edge_dict['uuid']
assert 'belief' in edge_dict
assert isinstance(edge_dict['belief'], (float, int))
assert stmt.belief == edge_dict['belief']
def test_transphosphorylation():
egfr = Agent('EGFR', db_refs={'HGNC': id('EGFR')})
egfr_dimer = Agent('EGFR',
bound_conditions=[BoundCondition(egfr)],
db_refs={'HGNC': id('EGFR')})
stmt = Transphosphorylation(egfr_dimer, 'Y', '1173')
stmt_hash = stmt.get_hash(refresh=True)
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert belgraph.number_of_nodes() == 3
assert belgraph.number_of_edges() == 3
egfr_dimer_node = complex_abundance([egfr_dsl, egfr_dsl])
egfr_phos_node = egfr_dsl.with_variants(pmod('Ph', 'Tyr', 1173))
edge_data = get_edge_data(belgraph, egfr_dimer_node, egfr_phos_node)
assert edge_data == {
pc.RELATION: pc.DIRECTLY_INCREASES,
pc.ANNOTATIONS: {
'stmt_hash': {
stmt_hash: True
},
'uuid': {
stmt.uuid: True
},
'belief': {
stmt.belief: True
},
},
}, edge_data
def test_inhibition():
braf_kin = Agent('BRAF',
activity=ActivityCondition('kinase', True),
db_refs={
'HGNC': '1097',
'UP': 'P15056'
})
mek = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'})
stmt = Inhibition(braf_kin, mek, 'kinase')
stmt_hash = stmt.get_hash(refresh=True)
edge = {
pc.RELATION: pc.DECREASES,
pc.SUBJECT: activity('kin'),
pc.OBJECT: activity('kin'),
pc.ANNOTATIONS: {
'stmt_hash': {
stmt_hash: True
},
'uuid': {
stmt.uuid: True
},
'belief': {
stmt.belief: True
},
},
}
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert belgraph.number_of_nodes() == 2, belgraph.number_of_nodes()
assert braf_dsl in belgraph
assert map2k1_dsl in belgraph
assert belgraph.number_of_edges() == 1
edge_data = get_first_edge_data(belgraph)
assert edge_data == edge, edge_data
def test_bound_condition():
egfr = Agent('EGFR', db_refs={'HGNC': id('EGFR')})
grb2 = Agent('GRB2', db_refs={'HGNC': id('GRB2')})
ras = Agent('KRAS', db_refs={'HGNC': '6407'})
sos1_bound = Agent('SOS1', mods=[ModCondition('phosphorylation')],
bound_conditions=[BoundCondition(egfr), BoundCondition(grb2)],
db_refs={'HGNC': id('SOS1')})
stmt = Gef(sos1_bound, ras)
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert len(belgraph) == 6
assert belgraph.number_of_edges() == 5
# Don't bother to check the tuple, which is now generated by
# PyBEL directly, but check the node data
assert egfr_grb2_sos1_phos_complex_dsl in belgraph
assert kras_node in belgraph
assert (egfr_grb2_sos1_phos_complex_dsl, kras_node) in belgraph.edges()
edge_data = (egfr_grb2_sos1_phos_complex_dsl, kras_node,
{
pc.RELATION: pc.DIRECTLY_INCREASES,
pc.OBJECT: activity('gtp')
})
assert edge_data in belgraph.edges(data=True)
def test_simple_modification_no_evidence():
braf = Agent('BRAF', db_refs={'HGNC': '1097', 'UP': 'P15056'})
braf_kin = Agent('BRAF', activity=ActivityCondition('kinase', True),
db_refs={'HGNC': '1097', 'UP': 'P15056'})
braf_cat = Agent('BRAF', activity=ActivityCondition('catalytic', True),
db_refs={'HGNC': '1097', 'UP': 'P15056'})
map2k1 = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'}) # MEK
stmt1 = Phosphorylation(braf, map2k1, 'S', '218')
stmt2 = Phosphorylation(braf_kin, map2k1, 'S', '218')
stmt3 = Ubiquitination(braf_cat, map2k1, 'S', '218')
# Edge info for subject
edge1 = None
edge2 = activity('kin')
edge3 = activity('cat')
for stmt, modtuple, subj_edge in ((stmt1, phos_dsl, edge1),
(stmt2, phos_dsl, edge2),
(stmt3, ub_dsl, edge3)):
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert belgraph.number_of_nodes() == 3, belgraph.number_of_nodes()
map2k1_mod_dsl = map2k1_dsl.with_variants(modtuple)
assert set(belgraph) == {braf_dsl, map2k1_dsl, map2k1_mod_dsl}, \
(set(belgraph), {braf_dsl, map2k1_dsl, map2k1_mod_dsl})
assert belgraph.number_of_edges() == 2, belgraph.number_of_edges()
assert belgraph.has_edge(map2k1_dsl, map2k1_mod_dsl)
assert belgraph.has_edge(braf_dsl, map2k1_mod_dsl)
edge_data = get_edge_data(belgraph, braf_dsl, map2k1_mod_dsl)
assert edge_data[pc.RELATION] == pc.INCREASES
assert edge_data.get(pc.SUBJECT) == subj_edge
def test_direct_activation():
braf_no_act = Agent('BRAF', db_refs={'HGNC': '1097', 'UP': 'P15056'})
braf_kin = Agent('BRAF',
activity=ActivityCondition('kinase', True),
db_refs={
'HGNC': '1097',
'UP': 'P15056'
})
mek = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'})
stmt1_ev = Evidence(
pmid='1234',
epistemics={'direct': True},
)
stmt1 = Activation(braf_no_act, mek, evidence=stmt1_ev)
stmt2 = Activation(braf_kin, mek, 'kinase', evidence=stmt1_ev)
hash1 = stmt1.get_hash(refresh=True)
hash2 = stmt2.get_hash(refresh=True)
edge1 = {
pc.RELATION: pc.DIRECTLY_INCREASES,
pc.OBJECT: {
pc.MODIFIER: pc.ACTIVITY
},
pc.EVIDENCE: 'No evidence text.',
pc.CITATION: {
pc.CITATION_DB: pc.CITATION_TYPE_PUBMED,
pc.CITATION_IDENTIFIER: '1234',
},
pc.ANNOTATIONS: {
'stmt_hash': hash1,
'source_hash': stmt1_ev.get_source_hash(),
'uuid': stmt1.uuid,
'belief': stmt1.belief,
},
}
edge2 = {
pc.RELATION: pc.DIRECTLY_INCREASES,
pc.SUBJECT: activity('kin'),
pc.OBJECT: activity('kin'),
pc.EVIDENCE: 'No evidence text.',
pc.CITATION: {
pc.CITATION_DB: pc.CITATION_TYPE_PUBMED,
pc.CITATION_IDENTIFIER: '1234',
},
pc.ANNOTATIONS: {
'stmt_hash': hash2,
'source_hash': stmt1_ev.get_source_hash(),
'uuid': stmt2.uuid,
'belief': stmt2.belief,
},
}
for stmt, expected_edge in ((stmt1, edge1), (stmt2, edge2)):
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert belgraph.number_of_nodes() == 2, belgraph.number_of_nodes()
assert braf_dsl in belgraph
assert map2k1_dsl in belgraph
assert belgraph.number_of_edges() == 1
edge_data = get_first_edge_data(belgraph)
assert expected_edge == edge_data, json.dumps(edge_data, indent=1)
def test_modification_with_mutation():
braf = Agent('BRAF', mutations=[MutCondition('600', 'V', 'E')],
db_refs={'HGNC': '1097', 'UP': 'P15056'})
mek = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'})
stmt = Phosphorylation(braf, mek, 'S', '218')
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
# Adds in the base protein nodes as well as the variants (so 4 nodes)
assert belgraph.number_of_nodes() == 4, belgraph.number_of_nodes()
braf_mut_dsl = braf_dsl.with_variants(hgvs('p.Val600Glu'))
assert braf_mut_dsl in belgraph
def test_activation():
braf_no_act = Agent('BRAF', db_refs={'HGNC': '1097', 'UP': 'P15056'})
braf_kin = Agent('BRAF',
activity=ActivityCondition('kinase', True),
db_refs={
'HGNC': '1097',
'UP': 'P15056'
})
mek = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'})
stmt1 = Activation(braf_no_act, mek)
stmt2 = Activation(braf_kin, mek, 'kinase')
hash1 = stmt1.get_hash(refresh=True)
hash2 = stmt2.get_hash(refresh=True)
edge1 = {
pc.RELATION: pc.INCREASES,
pc.OBJECT: activity(),
pc.ANNOTATIONS: {
'stmt_hash': {
hash1: True
},
'uuid': {
stmt1.uuid: True
},
'belief': {
stmt1.belief: True
},
},
}
edge2 = {
pc.RELATION: pc.INCREASES,
pc.SUBJECT: activity('kin'),
pc.OBJECT: activity('kin'),
pc.ANNOTATIONS: {
'stmt_hash': {
hash2: True
},
'uuid': {
stmt2.uuid: True
},
'belief': {
stmt2.belief: True
},
},
}
for stmt, edge in ((stmt1, edge1), (stmt2, edge2)):
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert belgraph.number_of_nodes() == 2, belgraph.number_of_nodes()
assert braf_dsl in belgraph
assert map2k1_dsl in belgraph
assert belgraph.number_of_edges() == 1
edge_data = get_first_edge_data(belgraph)
assert edge_data == edge, edge_data
def test_complex():
egfr = Agent('EGFR', db_refs={'HGNC': id('EGFR')})
grb2 = Agent('GRB2', db_refs={'HGNC': id('GRB2')})
sos = Agent('SOS1', db_refs={'HGNC': id('SOS1')})
stmt = Complex([egfr, grb2, sos])
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
# The graph should contain the node for the complex as well as nodes
# for all of the members
assert len(belgraph) == 4
assert egfr_grb2_sos1_complex_dsl in belgraph
for member in egfr_grb2_sos1_complex_dsl.members:
assert member in belgraph
def test_increase_amount():
tp53 = Agent('TP53', db_refs={'HGNC': '11998'})
mdm2 = Agent('MDM2', db_refs={'HGNC': '6973'})
stmt = IncreaseAmount(tp53, mdm2)
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert belgraph.number_of_nodes() == 2, belgraph.number_of_nodes()
assert mdm2_dsl in belgraph
assert tp53_dsl in belgraph
assert belgraph.number_of_edges() == 1
edge_data = get_first_edge_data(belgraph)
assert edge_data[pc.RELATION] == pc.INCREASES
def test_increase_amount_tscript():
tp53 = Agent('TP53', activity=ActivityCondition('transcription', True),
db_refs={'HGNC': '11998'})
mdm2 = Agent('MDM2', db_refs={'HGNC': '6973'})
stmt = IncreaseAmount(tp53, mdm2)
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert belgraph.number_of_nodes() == 2, belgraph.number_of_nodes()
assert mdm2_dsl in belgraph
assert tp53_dsl in belgraph
assert belgraph.number_of_edges() == 1
edge_data = get_first_edge_data(belgraph)
assert edge_data[pc.RELATION] == pc.INCREASES
assert edge_data[pc.SUBJECT] == activity('tscript')
def test_inhibition():
braf_kin = Agent('BRAF', activity=ActivityCondition('kinase', True),
db_refs={'HGNC': '1097', 'UP': 'P15056'})
mek = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'})
stmt = Inhibition(braf_kin, mek, 'kinase')
edge = {pc.RELATION: pc.DIRECTLY_DECREASES,
pc.SUBJECT: activity('kin'),
pc.OBJECT: activity('kin')}
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert len(belgraph.nodes()) == 2
assert braf_dsl in belgraph
assert map2k1_dsl in belgraph
assert belgraph.number_of_edges() == 1
edge_data = get_first_edge_data(belgraph)
assert edge_data == edge
def test_rxn_no_controller():
glu = Agent('D-glucose', db_refs={'CHEBI': 'CHEBI:17634'})
g6p = Agent('D-glucopyranose 6-phosphate', db_refs={'CHEBI': 'CHEBI:4170'})
stmt = Conversion(None, [glu], [g6p])
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
# The graph should contain the node for the reaction as well as nodes
# for all of the members
assert chebi_17534_to_4170 in belgraph
for reactant in chebi_17534_to_4170.reactants:
assert reactant in belgraph
assert belgraph.number_of_nodes() == 3, belgraph.number_of_nodes()
# TODO check edge chebi_17534_to_4170 hasReactant chebi_17534
for product in chebi_17534_to_4170.products:
assert product in belgraph
def test_active_form():
ras = Agent('KRAS', mutations=[MutCondition('12', 'G', 'V')],
db_refs={'HGNC': '6407'})
mapk1_p = Agent('MAP2K1',
mods=[ModCondition('phosphorylation', 'T', '185')],
db_refs={'HGNC': hgnc_client.get_hgnc_id('MAP2K1')})
mapk1_pp = Agent('MAP2K1',
mods=[ModCondition('phosphorylation', 'T', '185'),
ModCondition('phosphorylation', 'Y', '187')],
db_refs={'HGNC': hgnc_client.get_hgnc_id('MAP2K1')})
stmt1 = ActiveForm(ras, 'gtpbound', True)
stmt2 = ActiveForm(mapk1_p, 'kinase', True)
stmt3 = ActiveForm(mapk1_pp, 'kinase', True)
for stmt in (stmt1, stmt2, stmt3):
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert len(belgraph) == 2
def test_rxn_no_controller():
glu = Agent('D-GLUCOSE', db_refs={'CHEBI': 'CHEBI:17634'})
g6p = Agent('GLUCOSE-6-PHOSPHATE', db_refs={'CHEBI': 'CHEBI:4170'})
stmt = Conversion(None, [glu], [g6p])
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
# The graph should contain the node for the reaction as well as nodes
# for all of the members
assert len(belgraph) == 3
assert chebi_17534_to_4170 in belgraph
for reactant in chebi_17534_to_4170.reactants:
assert reactant in belgraph
# TODO check edge chebi_17534_to_4170 hasReactant chebi_17534
for product in chebi_17534_to_4170.products:
assert product in belgraph
def test_rxn_with_controller():
hk1 = Agent('HK1', db_refs={'HGNC': id('HK1')})
glu = Agent('D-GLUCOSE', db_refs={'CHEBI': 'CHEBI:17634'})
g6p = Agent('GLUCOSE-6-PHOSPHATE', db_refs={'CHEBI': 'CHEBI:4170'})
stmt = Conversion(hk1, [glu], [g6p])
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
# The graph should contain the node for the reaction as well as nodes
# for all of the members
assert len(belgraph) == 4
# check the catalyst makes it
assert protein(namespace='HGNC', name='HK1') in belgraph
# The reaction data should be the same as before
assert chebi_17534 in belgraph
assert chebi_4170 in belgraph
assert chebi_17534_to_4170 in belgraph
def test_no_activity_on_bioprocess():
yfg_agent = Agent('PPP1R13L', db_refs={'HGNC': id('PPP1R13L')})
apoptosis_agent = Agent('apoptotic process', db_refs={'GO': 'GO:0006915'})
stmt = Activation(yfg_agent, apoptosis_agent)
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert len(belgraph) == 2
assert belgraph.number_of_edges() == 1
yfg_pybel = protein('HGNC', 'PPP1R13L')
apoptosis_pybel = bioprocess('GO', 'GO:0006915')
assert yfg_pybel in belgraph
assert apoptosis_pybel in belgraph
_, _, e = list(belgraph.edges(data=True))[0]
assert pc.OBJECT not in e
def test_complex_with_pmod():
sos1_phos = Agent('SOS1',
mods=[ModCondition('phosphorylation', 'Y', '100')],
db_refs={'HGNC': id('SOS1')})
grb2 = Agent('GRB2', db_refs={'HGNC': id('GRB2')})
egfr = Agent('EGFR', db_refs={'HGNC': id('EGFR')})
stmt = Complex([sos1_phos, grb2, egfr])
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert belgraph.number_of_nodes() == 5
assert belgraph.number_of_edges() == 4
egfr_grb2_sos_phos_tyr_100 = complex_abundance(
[egfr_dsl, grb2_dsl,
sos1_dsl.with_variants(pmod('Ph', 'Tyr', 100))])
assert sos1_dsl in belgraph
assert egfr_grb2_sos_phos_tyr_100 in belgraph
for member in egfr_grb2_sos_phos_tyr_100.members:
assert member in belgraph
def test_rxn_with_controller():
hk1 = Agent('HK1', db_refs={'HGNC': id('HK1')})
glu = Agent('D-glucose', db_refs={'CHEBI': 'CHEBI:17634'})
g6p = Agent('D-glucopyranose 6-phosphate', db_refs={'CHEBI': 'CHEBI:4170'})
stmt = Conversion(hk1, [glu], [g6p])
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
# check the catalyst makes it
assert protein(namespace='HGNC', name='HK1', identifier=id('HK1')) \
in belgraph
# The reaction data should be the same as before
assert chebi_17534 in belgraph
assert chebi_4170 in belgraph
assert chebi_17534_to_4170 in belgraph
# The graph should contain the node for the reaction as well as nodes
# for all of the members
assert belgraph.number_of_nodes() == 4, belgraph.number_of_nodes()
def test_direct_activation():
braf_no_act = Agent('BRAF', db_refs={'HGNC': '1097', 'UP': 'P15056'})
braf_kin = Agent('BRAF', activity=ActivityCondition('kinase', True),
db_refs={'HGNC': '1097', 'UP': 'P15056'})
mek = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'})
stmt1_ev = Evidence(
pmid='1234',
epistemics={'direct': True},
)
stmt1 = Activation(braf_no_act, mek, evidence=stmt1_ev)
stmt2 = Activation(braf_kin, mek, 'kinase', evidence=stmt1_ev)
edge1 = {
pc.RELATION: pc.DIRECTLY_INCREASES,
pc.OBJECT: {pc.MODIFIER: pc.ACTIVITY},
pc.EVIDENCE: 'No evidence text.',
pc.CITATION: {
pc.CITATION_TYPE: pc.CITATION_TYPE_PUBMED,
pc.CITATION_REFERENCE: '1234',
},
}
edge2 = {
pc.RELATION: pc.DIRECTLY_INCREASES,
pc.SUBJECT: activity('kin'),
pc.OBJECT: activity('kin'),
pc.EVIDENCE: 'No evidence text.',
pc.CITATION: {
pc.CITATION_TYPE: pc.CITATION_TYPE_PUBMED,
pc.CITATION_REFERENCE: '1234',
},
}
for stmt, expected_edge in ((stmt1, edge1), (stmt2, edge2)):
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert len(belgraph.nodes()) == 2
assert braf_dsl in belgraph
assert map2k1_dsl in belgraph
assert belgraph.number_of_edges() == 1
edge_data = get_first_edge_data(belgraph)
assert expected_edge == edge_data
def test_modification_with_evidences():
braf_kin = Agent('BRAF', activity=ActivityCondition('kinase', True),
db_refs={'HGNC': '1097', 'UP': 'P15056'})
mek = Agent('MAP2K1', db_refs={'HGNC': '6840', 'UP': 'Q02750'})
evidence = Evidence(source_api='test', text='evidence text', pmid='1234')
stmt = Phosphorylation(braf_kin, mek, 'S', '218', evidence=evidence)
pba = pa.PybelAssembler([stmt])
belgraph = pba.make_model()
assert len(belgraph.nodes()) == 3
assert braf_dsl in belgraph
map2k1_mod_dsl = map2k1_dsl.with_variants(phos_dsl)
assert map2k1_mod_dsl in belgraph
assert belgraph.number_of_edges() == 2
edge_data = get_edge_data(belgraph, braf_dsl, map2k1_mod_dsl)
assert edge_data.get(pc.SUBJECT) == activity('kin')
assert edge_data[pc.RELATION] == pc.INCREASES
assert edge_data[pc.EVIDENCE] == 'evidence text'
assert edge_data[pc.CITATION] == {
pc.CITATION_TYPE: pc.CITATION_TYPE_PUBMED,
pc.CITATION_REFERENCE: '1234',
}
assert 'source_api' in edge_data[pc.ANNOTATIONS]
assert edge_data[pc.ANNOTATIONS]['source_api'] == 'test'
assert 'source_id' not in edge_data[pc.ANNOTATIONS]
