@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8
> .
@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:NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8130_head
{
this:
np:hasAssertion
dgn-np:NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8130_assertion
;
np:hasProvenance
dgn-np:NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8130_provenance
;
np:hasPublicationInfo
dgn-np:NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8130_assertion
a
np:Assertion
.
dgn-np:NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8130_provenance
a
np:Provenance
.
dgn-np:NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0032460
a
ncit:C7057
.
dgn-gda:DGN967fdb5d4bdd3488fb02a81ff545d9d2
sio:SIO_000628
miriam-gene:3630
,
lld:C0032460
;
a
sio:SIO_001121
.
}
dgn-np:NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8130_provenance
{
dgn-np:NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8130_assertion
dcterms:description
"[Variation at the insulin gene VNTR (variable number tandem repeat) minisatellite has been reported to be associated with polycystic ovary syndrome (PCOS), but findings have been inconsistent and all studies have featured small sample sizes.]. 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:15705917
;
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:NP191706.RA2Jd12DgJRxQMBOJJqoVZGajw4KpPW7TvW-vfIFLsqB8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}