@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0> .
@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:NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0130_head {
  this: np:hasAssertion dgn-np:NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0130_assertion;
    np:hasProvenance dgn-np:NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0130_provenance;
    np:hasPublicationInfo dgn-np:NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0130_assertion a np:Assertion .
  
  dgn-np:NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0130_provenance a np:Provenance .
  
  dgn-np:NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN38586b525c81a3a61927347a19a1fcff sio:SIO_000628 miriam-gene:5728, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0130_provenance {
  dgn-np:NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0130_assertion dcterms:description
      "[We show significant association between ERG gene rearrangements and PTEN genomic aberrations in subset of PCA. Our analysis also provides further support for the observation that homozygous PTEN deletions can occur within the subset of HGPIN lesions, and shows accumulating genetic aberrations with disease progression, evidenced by higher detection in PCA than in HGPIN and more PTEN homozygous deletions in GS 8-10 than in 6-7.]. 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:20590547;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP67852.RASvSjCyJ_M0KNVjRnpAbUYIgevm_AaMcXGd1q6uGG0F0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}