@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w> .
@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:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_head {
  this: np:hasAssertion dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_assertion;
    np:hasProvenance dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_provenance;
    np:hasPublicationInfo dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_assertion a np:Assertion .
  
  dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_provenance a np:Provenance .
  
  dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_assertion {
  miriam-gene:57045 a ncit:C16612 .
  
  lld:C0600139 a ncit:C7057 .
  
  dgn-gda:DGNf662c043473d8a88f4de390627d7bef8 sio:SIO_000628 miriam-gene:57045, lld:C0600139;
    a sio:SIO_001121 .
}

dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_provenance {
  dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_assertion dcterms:description
      "[Molecular genetic analyses of human prostate cancer (CaP) has revealed frequent loss of specific chromosome regions suggesting the presence of putative tumor suppressor gene(s) (TSG) on these chromosome loci whose inactivation may play a role in prostate tumorigenesis.]. 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:10371356;
    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:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:06+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" .
}