@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE> .
@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 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:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_head {
  this: np:hasAssertion dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_assertion;
    np:hasProvenance dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_provenance;
    np:hasPublicationInfo dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_assertion a np:Assertion .
  
  dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_provenance a np:Provenance .
  
  dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0162311 a ncit:C7057 .
  
  dgn-gda:DGN59609fed5f1cb47fb6a92e13308125fe sio:SIO_000628 miriam-gene:367, lld:C0162311;
    a sio:SIO_001122 .
}

dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_provenance {
  dgn-np:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_assertion dct:description
      "[To determine if the androgen receptor gene is associated with male pattern baldness, we compared allele frequencies of the androgen receptor gene polymorphisms (StuI restriction fragment length polymorphism and two triplet repeat polymorphisms) in cases with cosmetically significant baldness (54 young and 392 older men) and controls (107 older men) with no indication of baldness.]. 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:11231320;
    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:NP48055.RAmuzoTB32u3Phe6LirZBZVTy3NcMiRhR0HbxFRg0tENE130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}