@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk> .
@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:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_head {
  this: np:hasAssertion dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_assertion ;
    np:hasProvenance dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_provenance ;
    np:hasPublicationInfo dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_assertion a np:Assertion .
  dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_provenance a np:Provenance .
  dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_assertion {
  miriam-gene:3643 a ncit:C16612 .
  lld:C0206081 a ncit:C7057 .
  dgn-gda:DGN328806f15d009223c63178de1e7e8b60 sio:SIO_000628 miriam-gene:3643 , lld:C0206081 ;
    a sio:SIO_001121 .
}
dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_provenance {
  dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_assertion dcterms:description "[This evidence includes: (1) mutations in the insulin receptor gene that cause severe hyperinsulinemia appear to be associated with ovarian hyperandrogenism, (2) insulin stimulates ovarian thecal and stromal androgen secretion in vitro, and (3) in some experimental models, manipulation of circulating insulin concentrations results in changes in circulating androgens.]. 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:8064699 ;
    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:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:24+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" .
}