@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ130_head
{
this:
np:hasAssertion
dgn-np:NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ130_assertion
;
np:hasProvenance
dgn-np:NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ130_assertion
a
np:Assertion
.
dgn-np:NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ130_provenance
a
np:Provenance
.
dgn-np:NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ130_assertion
{
miriam-gene:1583
a
ncit:C16612
.
lld:C0032460
a
ncit:C7057
.
dgn-gda:DGNd0d4b7abcf93fedcb3700b63d43227f0
sio:SIO_000628
miriam-gene:1583
,
lld:C0032460
;
a
sio:SIO_001121
.
}
dgn-np:NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ130_provenance
{
dgn-np:NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ130_assertion
dcterms:description
"[The results of both linkage and association studies suggest that CYP11a (coding for P450 cholesterol side chain cleavage) and the insulin VNTR regulatory polymorphism are important genes in the aetiology of PCOS and may explain, in part, the heterogeneity of the syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:9922108
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP385654.RAYoP9fHTLdybE0iodvPzIuk5nCpi1BViyN3x13Gl8lKQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:49+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}