@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ
> .
@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:NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ130_head
{
this:
np:hasAssertion
dgn-np:NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ130_assertion
;
np:hasProvenance
dgn-np:NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ130_assertion
a
np:Assertion
.
dgn-np:NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ130_provenance
a
np:Provenance
.
dgn-np:NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C0032460
a
ncit:C7057
.
dgn-gda:DGN69c3dfe327f3e75440b842e41eed45f0
sio:SIO_000628
miriam-gene:1586
,
lld:C0032460
;
a
sio:SIO_001122
.
}
dgn-np:NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ130_provenance
{
dgn-np:NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ130_assertion
dcterms:description
"[Data show that the frequency of seven single nucleotide polymorphisms of CYP17A1 studied had no significant association with polycystic ovary syndrome, but one haplotype may be associated with the pathogenesis of PCOS in a Korean population.]. 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:18636181
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP123602.RAoN0tVmEazniU3dmZCTdVrvuvUWU0RJnPkJwpRDrsKiQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:04+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" .
}