@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" .
}