@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo> .
@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:NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo130_head {
  this: np:hasAssertion dgn-np:NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo130_assertion;
    np:hasProvenance dgn-np:NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo130_provenance;
    np:hasPublicationInfo dgn-np:NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo130_assertion a np:Assertion .
  
  dgn-np:NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo130_provenance a np:Provenance .
  
  dgn-np:NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C1839259 a ncit:C7057 .
  
  dgn-gda:DGN4b08299707ab92f0229e06ec51ee8ffd sio:SIO_000628 miriam-gene:367, lld:C1839259;
    a sio:SIO_001121 .
}

dgn-np:NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo130_provenance {
  dgn-np:NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo130_assertion dcterms:description
      "[This review summarizes the most recent information on two pathologies linked to mutations of the androgen receptor, namely, the complete androgen insensitivity syndrome (CAIS) and the spinal and bulbar muscular atrophy (SBMA or Kennedy's disease).]. 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:16388114;
    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:NP529132.RA5pBi2qKorSOFJh2BTHGd4-YjBwPn65TfRFNTp7oEeoo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:44+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" .
}