def _siphon_family_interactions(self, triples):
ints = []
FIELDS = ("FAM", "ID", "INT_TYPE")
for row in iterate_csv(self._get_path("homodomain_interaction.csv",
is_db=False),
num_skip=1,
delimiter="\t",
fieldnames=FIELDS):
ints.append((row["FAM"], row["FAM"], row["INT_TYPE"]))
FIELDS = ("FAM1", "ID1", "FAM2", "ID2", "INT_TYPE")
for row in iterate_csv(self._get_path("heterodomain_interaction.csv",
is_db=False),
num_skip=1,
delimiter="\t",
fieldnames=FIELDS):
ints.append((row["FAM1"], row["FAM2"], row["INT_TYPE"]))
int_types = set()
for fam1, fam2, int_type in ints:
fam1 = O.uri(O.PFAM_ID, fam1)
fam2 = O.uri(O.PFAM_ID, fam2)
int_type = O.uri(O.IPFAM_INT_TYPE, int_type)
blank = B()
triples.extend([
(blank, O.RDF.type, O.IPFAM_INT),
(blank, O.IPFAM_INT_HAS_INT_TYPE, int_type),
(blank, O.IPFAM_INT_HAS_PFAM, fam1),
(blank, O.IPFAM_INT_HAS_PFAM, fam2),
])
self._add_if_new(triples, int_types, int_type, O.RDF.type,
O.IPFAM_INT_TYPE)
del ints
def _siphon_regions(self, triples):
FIELDS = (
"REGION", # int(10)
"PROT_FAM", # int(11)
"PROT_FAM_ACC", # varchar(45)
"PDB_ID", # varchar(4)
"CHAIN", # varchar(1)
"START", # int(11)
"START_ICODE", # varchar(1)
"END", # int(11)
"END_ICODE", # varchar(1)
"REGION_SOURCE_DB", # varchar(12)
)
for row in iterate_csv(self._get_path("pdb_protein_region.txt"),
delimiter="\t",
fieldnames=FIELDS):
region = O.uri(O.IPFAM_REGION, row["REGION"])
pfam = O.uri(O.PFAM_ID, row["PROT_FAM_ACC"])
pdb_id_chain = U(O.PDBR + row["PDB_ID"].lower() + "_" +
row["CHAIN"])
triples.extend([
(region, O.RDF.type, O.IPFAM_REGION),
(region, O.IPFAM_REGION_INSTANCE_OF, pfam),
(region, O.IPFAM_REGION_OCCURS_IN, pdb_id_chain),
(region, O.IPFAM_REGION_STARTS_AT, L(int(row["START"]))),
(region, O.IPFAM_REGION_STOPS_AT, L(int(row["END"]))),
])
def _siphon_cog(self, triples):
FIELDS = ("TAXON.STRING_ID", "START", "STOP", "CLUSTER_ID",
"ANNOTATION")
path = self._get_path("COG.mappings.v{}.txt").format(self._version)
for row in iterate_csv(path,
delimiter="\t",
fieldnames=FIELDS,
num_skip=1):
parts = row["TAXON.STRING_ID"].split(".")
taxon = parts[0]
string_id = ".".join(parts[1:])
if taxon != self._taxon:
continue
string_id = O.uri(O.STRING_ID, string_id)
cluster_id = row["CLUSTER_ID"]
if cluster_id.startswith("COG"):
cluster_id = O.uri(O.COG_CLUSTER_ID, cluster_id)
triples.extend([(string_id, O.STRING_ID_IN_COG, cluster_id),
(cluster_id, O.RDF.type, O.COG_CLUSTER_ID)])
elif cluster_id.startswith("KOG"):
cluster_id = O.uri(O.KOG_CLUSTER_ID, cluster_id)
triples.extend([(string_id, O.STRING_ID_IN_KOG, cluster_id),
(cluster_id, O.RDF.type, O.COG_CLUSTER_ID)])
elif cluster_id.startswith("NOG"):
cluster_id = O.uri(O.NOG_CLUSTER_ID, cluster_id)
triples.extend([(string_id, O.STRING_ID_IN_NOG, cluster_id),
(cluster_id, O.RDF.type, O.COG_CLUSTER_ID)])
def _siphon_domains(self, triples):
"""Converts the `domains.tab` file.
The data comes from an InterPro scan over the SGD entries.
"""
FIELDS = (
"FEAT_NAME", # S. cerevisiae systematic name (ID of the input sequence)
"CRC64", # CRC of the proteic sequence
"LENGTH", # Lenght of the sequence in AA
"METHOD", # Analysis method
"DB_MEMBERS", # DB members entry for this match
"DB_DESCRIPTION", # DB member description for the entry
"START", # start of the domain match
"STOP", # end of the domain match
"EVALUE", # E-value of the match (defined by DB)
"STATUS", # Status of the match: T=true, ?=unknown
"DATE", # Date of the run
"IPR_ID", # InterPro ID
"IPR_DESCRIPTION", # InterPro description
"IPR_GO", # GO description of the InterPro entry
)
for row in iterate_csv(self._get_path("domains.tab"),
delimiter="\t",
fieldnames=FIELDS):
feat_id = O.uri(O.SGD_FEATURE, self._sanitize(row["FEAT_NAME"]))
is_true = L({"T": True, "?": False}[row["STATUS"]])
db_id = L(None)
if row["METHOD"] == "Pfam" and row["STATUS"] == "T":
db_id = O.uri(O.PFAM_ID, row["DB_MEMBERS"])
try:
evalue = L(float(row["EVALUE"]))
except ValueError:
evalue = L(-1.0)
_ = B()
triples.extend([
(_, O.RDF.type, O.SGD_IPR_HIT),
(_, O.SGD_IPR_HIT_HAS_ID, L(row["IPR_ID"])),
(_, O.SGD_IPR_HIT_HAS_METHOD, L(row["METHOD"])),
(_, O.SGD_IPR_HIT_HAS_DB_ID, db_id),
(_, O.SGD_IPR_HIT_STARTS_AT, L(int(row["START"]))),
(_, O.SGD_IPR_HIT_STOPS_AT, L(int(row["STOP"]))),
(_, O.SGD_IPR_HIT_HAS_EVALUE, evalue),
(_, O.SGD_IPR_HIT_IS_TRUE, is_true),
(feat_id, O.SGD_FEATURE_HAS_IPR_HIT, _),
])
def _siphon_pdb_homologues(self, triples):
"""Converts the `pdb_homologs.tab` file."""
FIELDS = (
"FEAT_NAME", # S. cerevisiae systematic name
"START_COORD_QUERY", # start coord (aa position) in yeast
"STOP_COORD_QUERY", # stop coord (aa position) in yeast
"START_COORD_TARGET", # start coord (aa position) in target
"STOP_COORD_TARGET", # stop coord (aa position) in target
"PERCENT_ALIGNED", # percent of yeast contained in target
"SCORE", # log of the expectation value
"TARGET_PDB_ID", # PDB identifier
"TARGET_TAXON_ID", # target taxon ID
"TARGET_TAXON_NAME", # target taxon species name
)
for row in iterate_csv(self._get_path("pdb_homologs.tab"),
delimiter="\t",
fieldnames=FIELDS):
pdb_id_chain, _ = self._pdb_to_uri(row["TARGET_PDB_ID"])
match = B()
triples.extend([
(match, O.RDF.type, O.SGD_PDB_HOMOLOGY),
(match, O.SGD_PDB_HAS_QUERY,
O.uri(O.SGD_FEATURE, row["FEAT_NAME"])),
(match, O.SGD_PDB_ALIGNMENT,
L(float(row["PERCENT_ALIGNED"]) / 100.0)),
(match, O.SGD_PDB_HAS_TARGET, pdb_id_chain),
])
def _siphon_aliases(self, triples):
from urllib2 import urlopen
BOXES = (
#( 0, 75, "GD"), # Gene designation
( 75, 95, "OLN"), # Ordered locus name
( 95, 106, "SP_ACC"), # Swiss-Prot accession
#(106, 118, "SP_NAME"), # Swiss-Prot entry name
#(118, 128, "SGD_ACCESSION"),# SGD accession
# XXX there are three more fields we do not care about
)
try:
url = urlopen("http://www.uniprot.org/docs/yeast.txt")
state = 0
for line in url.read().split("\n"):
if "____" in line or "----" in line:
state += 1
elif state == 5:
parts = { box[2]: map(str.strip, line[box[0]:box[1]].strip().split(";")) for box in BOXES }
assert len(parts["OLN"]) == 1
assert len(parts["SP_ACC"]) == 1
yip_acc = O.uri(O.YIP_PROTEIN, parts["OLN"][0])
sp_acc = U(O.UNIPROT_ID + parts["SP_ACC"][0])
triples.append((yip_acc, O.OWL.sameAs, sp_acc))
url.close()
except Exception, e:
print e
def _siphon_interactions(self, triples):
FIELDS = ("ITEM_ID_A", "ITEM_ID_B", "MODE", "ACTION", "A_IS_ACTING",
"SCORE", "SOURCES", "TRANSFERRED_SOURCES")
path = self._get_path("{}.protein.actions.detailed.v{}.txt") \
.format(self._taxon, self._version)
for row in iterate_csv(path,
delimiter="\t",
fieldnames=FIELDS,
num_skip=1):
id_a, id_b = row["ITEM_ID_A"], row["ITEM_ID_B"]
if not (id_a.startswith("{}".format(self._taxon)) and \
id_b.startswith("{}".format(self._taxon))):
continue
id_a = O.uri(O.STRING_ID, id_a.split(".", 1)[1])
id_b = O.uri(O.STRING_ID, id_b.split(".", 1)[1])
mode = O.uri(O.STRING_ACTION_MODE, row["MODE"])
triples.append((id_a, mode, id_b))
def _siphon_aliases(self, triples):
FIELDS = ("TAXON", "STRING_ID", "ALIAS_ID", "ALIAS_TYPE")
path = self._get_path("{}.protein.aliases.v{}.txt") \
.format(self._taxon, self._version)
for row in iterate_csv(path,
delimiter="\t",
fieldnames=FIELDS,
num_skip=1):
string_id = O.uri(O.STRING_ID, row["STRING_ID"])
triples.append((string_id, O.RDF.type, O.OCELOT.STRING_ID))
alias_id = row["ALIAS_ID"]
for alias_type in row["ALIAS_TYPE"].split():
if alias_type == "SGD" and \
(alias_id.startswith("S0") or alias_id.startswith("L0")):
db_alias_id = O.uri(O.SGD_ID, alias_id)
else:
# XXX handle UniProt ACs here
continue
triples.append((string_id, O.OWL.sameAs, db_alias_id))
def _siphon_sequences(self, triples):
"""Converts the `orf_trans_all.fasta` file."""
for header, sequence in read_fasta(
self._get_path("orf_trans_all.fasta")):
assert "SGDID:" in header
sgd_ids = filter(lambda word: word.startswith("SGDID:"),
header.split())
assert len(sgd_ids) == 1
sgd_id = O.uri(O.SGD_ID,
self._sanitize(sgd_ids[0].split(":")[1].strip(",")))
triples.append((sgd_id, O.SGD_ID_HAS_SEQUENCE, L(sequence)))
def _siphon_region_interactions(self, triples):
FIELDS = (
"REGION_INT", # `auto_reg_int` bigint(20) NOT NULL AUTO_INCREMENT,
"PDB_ID", # `pdb_id` varchar(4) NOT NULL,
"REGION_A", # `region_id_A` int(10) unsigned NOT NULL,
"REGION_B", # `region_id_B` int(10) unsigned NOT NULL,
"IS_INTRACHAIN", # `intrachain` tinyint(1) NOT NULL,
"QUALITY_CONTROL", # `quality_control` int(10) unsigned NOT NULL,
)
for row in iterate_csv(self._get_path("pdb_protein_region_int.txt"),
delimiter="\t",
fieldnames=FIELDS):
region_int = O.uri(O.IPFAM_REGION_INT, row["REGION_INT"])
region_a = O.uri(O.IPFAM_REGION, row["REGION_A"])
region_b = O.uri(O.IPFAM_REGION, row["REGION_B"])
pdb_id = U(O.PDBR + row["PDB_ID"].lower())
triples.extend([
(region_int, O.RDF.type, O.IPFAM_REGION_INT),
(region_int, O.IPFAM_REGION_INT_OCCURS_IN, pdb_id),
(region_int, O.IPFAM_REGION_INT_HAS_REGION, region_a),
(region_int, O.IPFAM_REGION_INT_HAS_REGION, region_b),
])
def _siphon_families(self, triples):
"""Converts the `protein_family.txt file."""
FIELDS = (
"FAMILY_INT", # `auto_prot_fam` int(11) NOT NULL AUTO_INCREMENT,
"FAMILY_ACC", # `accession` varchar(45) DEFAULT NULL,
"FAMILY_ID", # `identifier` varchar(45) DEFAULT NULL,
"DESCRIPTION", # `description` text,
"COMMENT", # `comment` longtext,
"FAMILY_TYPE", # `type` enum('family','domain','motif','repeat') DEFAULT NULL,
"SOURCE_DB", # `source_db` enum('pfama') DEFAULT NULL,
"COLOUR", # `colour` varchar(7) DEFAULT NULL,
"NUMBER_FAM_INT", # `number_fam_int` int(5) DEFAULT '0',
"NUMBER_LIG_INT", # `number_lig_int` int(5) DEFAULT '0',
"NUMBER_PDBS", # `number_pdbs` int(5) DEFAULT '0',
)
pfam_types = set()
for row in iterate_csv(self._get_path("protein_family.txt"),
num_skip=1,
delimiter="\t",
fieldnames=FIELDS):
assert len(row["FAMILY_ACC"]) > 0
if row["SOURCE_DB"] != "pfama":
print "Warning: invalid row '{}'".format(row.items())
continue
pfam_acc = O.uri(O.PFAM_ID, row["FAMILY_ACC"])
triples.append((pfam_acc, O.RDF.type, O.PFAM_ID))
if row["FAMILY_TYPE"] is None:
continue
if row["FAMILY_TYPE"]:
pfam_type = O.uri(O.PFAM_TYPE, row["FAMILY_TYPE"])
triples.append((pfam_acc, O.PFAM_ID_HAS_TYPE, pfam_type))
if not pfam_type in pfam_types:
pfam_types.add(pfam_type)
triples.append((pfam_type, O.RDF.type, O.PFAM_TYPE))
def _siphon_interactions(self, triples):
"""Converts the `interaction_data.tab` file."""
FIELDS = (
"BAIT_FEAT_NAME", # Bait: feature (ORF) name and gene name (optional)
"BAIT_STD_NAME", #
"HIT_FEAT_NAME", # Hit: feature (ORF) name and gene name (optional)
"HIT_STD_NAME", #
"EXPERIMENT_TYPE", # Description of the experiment
"INTERACTION_TYPE", # 'Genetic' or 'Physical'
"SOURCE_DATABASE", # Source database
"CURATION_TYPE", # Manual or high-throughput
"NOTES", # Free text (useless)
"PHENOTYPE", # Phenotype of the interaction (optional)
"REFERENCE", # List of references as 'SGD_REF:" (SGDID) or 'PMID:' (PubMed)
"CITATION", # List of citations
)
int_types, exp_types, cur_types, sources = set(), set(), set(), set()
for row in iterate_csv(self._get_path("interaction_data.tab"),
delimiter="\t",
fieldnames=FIELDS):
bait = O.uri(O.SGD_FEATURE, self._sanitize(row["BAIT_FEAT_NAME"]))
hit = O.uri(O.SGD_FEATURE, self._sanitize(row["HIT_FEAT_NAME"]))
int_type = O.uri(O.SGD_INT_TYPE,
self._sanitize(row["INTERACTION_TYPE"]))
exp_type = O.uri(O.SGD_INT_EXP_TYPE,
self._sanitize(row["EXPERIMENT_TYPE"]))
cur_type = O.uri(O.SGD_INT_CUR_TYPE,
self._sanitize(row["CURATION_TYPE"]))
source = O.uri(O.SGD_INT_SOURCE,
self._sanitize(row["SOURCE_DATABASE"]))
self._add_if_new(triples, int_types, int_type, O.RDF.type,
O.SGD_INT_TYPE)
self._add_if_new(triples, exp_types, exp_type, O.RDF.type,
O.SGD_INT_EXP_TYPE)
self._add_if_new(triples, cur_types, cur_type, O.RDF.type,
O.SGD_INT_CUR_TYPE)
self._add_if_new(triples, source, source, O.RDF.type,
O.SGD_INT_SOURCE)
interaction = B()
triples.extend([
(interaction, O.RDF.type, O.SGD_INT),
(interaction, O.SGD_INT_HAS_BAIT, bait),
(interaction, O.SGD_INT_HAS_HIT, hit),
(interaction, O.SGD_INT_HAS_TYPE, int_type),
(interaction, O.SGD_INT_HAS_EXP_TYPE, exp_type),
(interaction, O.SGD_INT_HAS_CUR_TYPE, cur_type),
(interaction, O.SGD_INT_HAS_SOURCE, source),
])
def _siphon_goslims(self, triples):
"""Converts the `go_slim_mapping.tab` file."""
# XXX there are a few goslim annotations with commas
FIELDS = (
"GENE_ORF", # Systematic gene name
"GENE_STD", # Gene name (optional)
"SGD_ID", # Gene SGD ID
"GO_ASPECT", # P = Process, F = Function, C = Component
"GO_TERM", # GO SLIM term
"GO_ID", # GO term ID
"FEATURE_TYPE", # Such as 'ORF' or 'tRNA'
)
for row in iterate_csv(self._get_path("go_slim_mapping.tab"),
delimiter="\t",
fieldnames=FIELDS):
if row["GO_TERM"] in ("other", "not_yet_annotated"):
continue
assert len(row["GO_ID"]), row
sgd_id = O.uri(O.SGD_ID, self._sanitize(row["SGD_ID"]))
goslim = O.go_to_uri(self._sanitize(row["GO_ID"]))
triples.append((sgd_id, O.SGD_ID_HAS_GOSLIM, goslim))
def _siphon_xrefs(self, triples):
"""Converts the `dbxref.tab` file."""
FIELDS = (
"XREF_ID", # Cross-reference ID
"XREF_ID_SOURCE", # Cross-reference database ID
"XREF_ID_TYPE", # Cross-reference type (like 'PDB chain' or 'PDB best hit')
"FEAT_NAME", # ORF name
"SGD_ID", # SGD ID
"UNDOCUMENTED", # Undocumented
)
for row in iterate_csv(self._get_path("dbxref.tab"),
delimiter="\t",
fieldnames=FIELDS):
sgd_id = O.uri(O.SGD_ID, self._sanitize(row["SGD_ID"]))
xref_source = self._sanitize(row["XREF_ID_SOURCE"])
xref_type = self._sanitize(row["XREF_ID_TYPE"])
if (xref_source, xref_type) == ("EBI", self._sanitize("UniProt/TrEMBL ID")) or \
(xref_source, xref_type) == ("EBI", self._sanitize("UniProt/Swiss-Prot ID")):
xref_id = O.UNIPROT_ID + row["XREF_ID"]
else:
continue
triples.append((sgd_id, O.SGD_ID_HAS_XREF, xref_id))
def _siphon_gos(self, triples):
"""Converts the `gene_association.sgd` file."""
FIELDS = (
"DB", # always "SGD"
"SGD_ID", # SGD ID
"DONTCARE_ID", # yeah
"QUALIFIERS", # Stuff like NOT, contributes_to, colocalizes; pipe-separated
"GO_ID", # GO term ID
"DB_REFS", # DB references; pipe-separated
"ECODE", # Evidence code for the annotation
"WITH_FROM", # With or From optional qualifiers
"GO_ASPECT", # P = Process, F = Function, C = Component
"DB_NAMES", # DB object names; pipe-separated
"DB_SYNONYMS", # DB synonyms; pipe-separated
"DB_TYPES", # DB object types; pipe-separated
"TAXIDS", # Taxon IDs; pipe-separated
"DATE", # Date the GO annotation was defined in YYYYMMDD
"ASSIGNED_BY", # always "SGD"
"EXTENSION", # yeah
"VARIANTS", # yeah
)
for row in iterate_csv(self._get_path("gene_association.sgd"),
num_skip=26,
delimiter="\t",
fieldnames=FIELDS):
assert len(row["SGD_ID"]), row
assert len(row["GO_ID"]), row
sgd_id = O.uri(O.SGD_ID, self._sanitize(row["SGD_ID"]))
go_term = O.go_to_uri(self._sanitize(row["GO_ID"]))
annotation = B()
triples.extend([
(annotation, O.RDF.type, O.SGD_GO_ANNOTATION),
(annotation, O.SGD_GO_ANNOTATION_HAS_SGD_ID, sgd_id),
(annotation, O.SGD_GO_ANNOTATION_HAS_TERM, go_term),
(annotation, O.SGD_GO_ANNOTATION_HAS_ECODE, L(row["ECODE"])),
])
def _siphon_features(self, triples):
"""Converts the `SGD_features.tab` file."""
# XXX there may be chromosomes not marked as features
FIELDS = (
"SGD_ID", # Primary SGD ID
"FEAT_TYPE", # Feature type
"FEAT_QUALIFIER", # Feature qualifier (optional)
"FEAT_NAME", # Feature name (optional)
"STD_GENE_NAME", # Standard gene name (optional)
"ALIASES", # Aliases (optional, |-separated)
"PARENT_FEAT_NAME", # Parent feature name (optional)
"OTHER_SGD_IDS", # Secondary SGD IDs (optional, |-separated)
"CHROMOSOME", # Chromosome (optional)
"START_COORD", # Start coordinate (optional)
"STOP_COORD", # Stop coordinate (optional)
"STRAND", # Strand (optional)
"GENETIC_POS", # Genetic position (optional)
"COORD_VERSION", # Coordinate version (optional)
"SEQ_VERSION", # Sequence version (optional)
"DESCRIPTION", # Description (optional)
)
feat_types, qualifiers, chromosomes = set(), set(), set()
for row in iterate_csv(self._get_path("SGD_features.tab"),
delimiter="\t",
fieldnames=FIELDS):
sgd_id = O.uri(O.SGD_ID, self._sanitize(row["SGD_ID"]))
feat_id = O.uri(O.SGD_FEATURE, self._sanitize(row["FEAT_NAME"]))
feat_type = O.uri(O.SGD_FEATURE_TYPE,
self._sanitize(row["FEAT_TYPE"]))
triples.extend([
(sgd_id, O.RDF.type, O.SGD_ID),
(feat_id, O.RDF.type, O.SGD_FEATURE),
(sgd_id, O.OWL.sameAs, feat_id),
(sgd_id, O.SGD_ID_HAS_TYPE, feat_type),
])
self._add_if_new(triples, feat_types, feat_type, O.RDF.type,
O.SGD_FEATURE_TYPE)
for q in filter(lambda q: len(q),
self._sanitize_all(row["FEAT_QUALIFIER"])):
q = O.uri(O.SGD_ID_QUALIFIER, q)
self._add_if_new(triples, qualifiers, q, O.RDF.type,
O.SGD_ID_QUALIFIER)
triples.append((sgd_id, O.SGD_ID_HAS_QUALIFIER, q))
for a in filter(lambda a: len(a),
self._sanitize_all(row["OTHER_SGD_IDS"])):
triples.append((sgd_id, O.OWL.sameAs, O.uri(O.SGD_ID, a)))
parent = row["PARENT_FEAT_NAME"]
if len(parent):
parent = O.uri(O.SGD_FEATURE, self._sanitize(parent))
triples.extend([
(parent, O.RDF.type, O.SGD_FEATURE),
(sgd_id, O.DCTERMS.isPartOf, parent),
])
chromosome = row["CHROMOSOME"]
if len(chromosome):
chromosome = O.uri(O.SGD_FEATURE, "chrosomosome_" + chromosome)
self._add_if_new(triples, chromosomes, chromosome, O.RDF.type,
O.SGD_CHROMOSOME)
triples.append((sgd_id, O.SGD_ID_IN_CHROMOSOME, chromosome))
if len(row["STRAND"]):
triples.append((sgd_id, O.SGD_ID_IN_STRAND, L(row["STRAND"])))
if len(row["START_COORD"]):
triples.append(
(sgd_id, O.SGD_ID_STARTS_AT, L(int(row["START_COORD"]))))
if len(row["STOP_COORD"]):
triples.append(
(sgd_id, O.SGD_ID_STOPS_AT, L(int(row["STOP_COORD"]))))
def _siphon_ids(self, triples):
for path in glob(self._get_path("divided/mmCIF")):
pdb_id = O.uri(O.PDB_ID, f.split(".")[0])
triples.append((pdb_id, O.RDF.type, O.PDBID))
def _r_uri(p, d, r):
return O.uri(O.YIP_RESIDUE, p + "_" + d + "_" + r)
def _pfam_uri(d):
return O.uri(O.PFAM_ID, d)
def _d_uri(p, d):
return O.uri(O.YIP_DOMAIN, p + "_" + d)
def _sgd_uri(p):
return O.uri(O.SGD_FEATURE, p)
def _p_uri(p):
return O.uri(O.YIP_PROTEIN, p)
