@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk> .
@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:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_head {
  this: np:hasAssertion dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_assertion;
    np:hasProvenance dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_provenance;
    np:hasPublicationInfo dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_assertion a np:Assertion .
  
  dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_provenance a np:Provenance .
  
  dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_assertion {
  miriam-gene:6715 a ncit:C16612 .
  
  lld:C0032460 a ncit:C7057 .
  
  dgn-gda:DGN8e8f25e6fd5583b9da8e3abee3bf0a9b sio:SIO_000628 miriam-gene:6715, lld:C0032460;
    a sio:SIO_001121 .
}

dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_provenance {
  dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_assertion dcterms:description
      "[The objective of the study was to test the hypothesis that haplotypes in the SRD5A1 and SRD5A2 genes are risk factors for PCOS and the severity of hirsutism in affected women.]. 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:16849416;
    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:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:29+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" .
}