@prefix orcid: <http://orcid.org/> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs> .
@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 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:NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs130_head {
   this: np:hasAssertion dgn-np:NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs130_assertion ;
    np:hasProvenance dgn-np:NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs130_provenance ;
    np:hasPublicationInfo dgn-np:NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs130_assertion a np:Assertion .
  dgn-np:NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs130_provenance a np:Provenance .
  dgn-np:NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs130_assertion {
   miriam-gene:367 a ncit:C16612 .
  lld:C0039585 a ncit:C7057 .
  dgn-gda:DGNd56d72f25f6426716b4231bf41cc321c sio:SIO_000628 miriam-gene:367 , lld:C0039585 ;
    a sio:SIO_001122 .
}
dgn-np:NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs130_provenance {
   dgn-np:NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs130_assertion dc:description "[Several mutations have been described in the human androgen receptor gene including constitutional mutations in androgen insensitivity syndrome, somatic mutations in prostate cancer and triplet expansions in Kennedy's disease (Gottlieb et al.1997).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_curated ;
    sio:SIO_000772 miriam-pubmed:9554754 ;
    prov:wasDerivedFrom dgn-void:uniprot-2016 ;
    prov:wasGeneratedBy eco:ECO_0000218 .
  dgn-void:source_evidence_curated a eco:ECO_0000205 ;
    rdfs:comment "Gene-disease associations manually curated."@en ;
    rdfs:label "DisGeNET evidence - CURATED"@en .
  dgn-void:uniprot-2016 pav:importedOn "2016-01-25"^^xsd:date .
}
dgn-np:NP9720.RAuXhAa_BUaLGjX1tl0LcM8mxhZeLRanrheDqo3iyrNCs130_publicationInfo {
   this: dc:created "2016-05-13T12:41:54+02:00"^^xsd:dateTime ;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dc:rightsHolder dgn-void:IBIGroup ;
    dc:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}