@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0> .
@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:NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0130_head {
  this: np:hasAssertion dgn-np:NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0130_assertion;
    np:hasProvenance dgn-np:NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0130_provenance;
    np:hasPublicationInfo dgn-np:NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0130_assertion a np:Assertion .
  
  dgn-np:NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0130_provenance a np:Provenance .
  
  dgn-np:NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0021364 a ncit:C7057 .
  
  dgn-gda:DGN1362b784a8e35a85240dadbdaaacb709 sio:SIO_000628 miriam-gene:367, lld:C0021364;
    a sio:SIO_001122 .
}

dgn-np:NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0130_provenance {
  dgn-np:NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0130_assertion dcterms:description
      "[While the correlation between the CAG repeat length of the androgen receptor (AR) gene and idiopathic male infertility is still unclear, ethnic background of the population studied may play an important role in this association.]. 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:15888966;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP63702.RA82RyitEjmOvnDEQuMFrblK8oJkuD5uSf0A0htUoUwK0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}