@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM> .
@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:NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM130_head {
  this: np:hasAssertion dgn-np:NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM130_assertion;
    np:hasProvenance dgn-np:NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM130_provenance;
    np:hasPublicationInfo dgn-np:NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM130_assertion a np:Assertion .
  
  dgn-np:NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM130_provenance a np:Provenance .
  
  dgn-np:NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM130_assertion {
  miriam-gene:2118 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGNb4c8d1cca2bb097691389375b7c4780c sio:SIO_000628 miriam-gene:2118, lld:C0376358;
    a sio:SIO_001121 .
}

dgn-np:NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM130_provenance {
  dgn-np:NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM130_assertion dcterms:description
      "[In this study we evaluated the frequency of fusion between TMPRSS2 and ETS family members (ERG, ETV1, ETV4) in prostate cancers in patients from northern China in order to explore differences in fusion rates among regions in northern and southern China, other parts of Asia, Europe, and North America.]. 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:23244085;
    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:NP519818.RABDYILLlLNSHAq_JJ2sn4uPr9M2YisDAGIlkdO22djyM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:09+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" .
}