@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM> .
@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/v3.0.0/void/> .

dgn-np:NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM130_head {
  this: np:hasAssertion dgn-np:NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM130_assertion;
    np:hasProvenance dgn-np:NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM130_provenance;
    np:hasPublicationInfo dgn-np:NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM130_assertion a np:Assertion .
  
  dgn-np:NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM130_provenance a np:Provenance .
  
  dgn-np:NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0153690 a ncit:C7057 .
  
  dgn-gda:DGN1b89e064fc841482b280fb9968572c24 sio:SIO_000628 miriam-gene:367, lld:C0153690;
    a sio:SIO_001122 .
}

dgn-np:NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM130_provenance {
  dgn-np:NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM130_assertion dcterms:description
      "[A relatively high frequency of the Thr868Ala mutation (originally reported for the human prostate cancer cell line androgen receptor) is particularly found in metastatic lesions (bone metastases) of prostate cancer and can be considered as a hot spot.]. 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:8717468;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP250458.RACJETa77cxuULgkLmPFgCy1HqCf22Y8nr7dt7gJwF6VM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:02+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}