@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs> .
@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:NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs130_head {
  this: np:hasAssertion dgn-np:NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs130_assertion;
    np:hasProvenance dgn-np:NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs130_provenance;
    np:hasPublicationInfo dgn-np:NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs130_assertion a np:Assertion .
  
  dgn-np:NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs130_provenance a np:Provenance .
  
  dgn-np:NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs130_assertion {
  miriam-gene:3757 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs130_provenance {
  dgn-np:NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs130_assertion dcterms:description
      "[To determine the relative order of genetic events in prostate carcinogenesis, we have analyzed 34 prostate carcinomas, 19 paired HGPIN lesions, 14 benign prostate hyperplasias, and 11 morphologically normal prostatic tissues for TMPRSS2-ERG and TMPRSS2-ETV1 rearrangements and genomic imbalances.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP178914.RAJJqqn8WgV20noXOTeQdm5tTUUTri8Z-YBL9LewRxVFs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:37+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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