@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g> .
@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:NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g130_head {
  this: np:hasAssertion dgn-np:NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g130_assertion;
    np:hasProvenance dgn-np:NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g130_provenance;
    np:hasPublicationInfo dgn-np:NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g130_assertion a np:Assertion .
  
  dgn-np:NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g130_provenance a np:Provenance .
  
  dgn-np:NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0242787 a ncit:C7057 .
  
  dgn-gda:DGNb330a05e3f9494af50ba4bbdc69c2b12 sio:SIO_000628 miriam-gene:367, lld:C0242787;
    a sio:SIO_001121 .
}

dgn-np:NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g130_provenance {
  dgn-np:NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g130_assertion dcterms:description
      "[Some AR ZFR point mutations observed in patients with partial androgen insensitivity syndrome or male breast cancer impair the interaction of AR with SNURF and also render AR refractory to the transcription-activating effect of SNURF.]. 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:10617653;
    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:NP673153.RAf7W9RoL-Cc2FMmA2XlilK6lZiQrxVFQ7FvUoq4kyR6g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:46+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" .
}