@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I130_head {
  this: np:hasAssertion dgn-np:NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I130_assertion;
    np:hasProvenance dgn-np:NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I130_provenance;
    np:hasPublicationInfo dgn-np:NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I130_assertion a np:Assertion .
  
  dgn-np:NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I130_provenance a np:Provenance .
  
  dgn-np:NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGNdf66978b466b78fbd884d0de6515e212 sio:SIO_000628 miriam-gene:367, lld:C0376358;
    a sio:SIO_001121 .
}

dgn-np:NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I130_provenance {
  dgn-np:NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I130_assertion dcterms:description
      "[Several diseases, such as androgen insensitivity syndrome (AIS), prostate cancer and spinal bulbar muscular atrophy (SBMA), have been shown to be associated with alterations in AR function due to mutations in the AR gene or dysregulation of androgen signalling.]. 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:21796517;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP912939.RAAkAQGLMeYGtG_qx77UbkatbBXbMP-aEGakVHrEjCy3I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:37+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}