@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE> .
@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:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_head {
  this: np:hasAssertion dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_assertion;
    np:hasProvenance dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_provenance;
    np:hasPublicationInfo dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_assertion a np:Assertion .
  
  dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_provenance a np:Provenance .
  
  dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_assertion {
  miriam-gene:79017 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGNef387e92190393580caa8df9905ddf4e sio:SIO_000628 miriam-gene:79017, lld:C0376358;
    a sio:SIO_001121 .
}

dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_provenance {
  dgn-np:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_assertion dcterms:description
      "[Several reports have suggested that one or both of the trinucleotide repeat polymorphisms in the human androgen receptor (hAR) gene, (CAG)n coding for polyglutamine and (GGC)n coding for polyglycine, may be associated with prostate cancer risk; but no study has investigated their association with disease progression.]. 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:10502720;
    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:NP312762.RALq8j61XALP9gHJvI9l1ZNJSSg6nGSjLASWwy9UZeqxE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:59+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" .
}