@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo> .
@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/v4.0.0/void/> .

dgn-np:NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo130_head {
  this: np:hasAssertion dgn-np:NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo130_assertion;
    np:hasProvenance dgn-np:NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo130_provenance;
    np:hasPublicationInfo dgn-np:NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo130_assertion a np:Assertion .
  
  dgn-np:NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo130_provenance a np:Provenance .
  
  dgn-np:NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo130_assertion {
  miriam-gene:5831 a ncit:C16612 .
  
  lld:C0600139 a ncit:C7057 .
  
  dgn-gda:DGNefab64c0992795637fa7ffeb6aa368fd sio:SIO_000628 miriam-gene:5831, lld:C0600139;
    a sio:SIO_001121 .
}

dgn-np:NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo130_provenance {
  dgn-np:NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo130_assertion dcterms:description
      "[These four variants, plus two other variants (PRO3 and INDEL1) that have been linked to prostate cancer risk in the previous studies, were typed for all study subjects, which included 130 prostate cancer cases, 130 patients with benign prostatic hyperplasia and 150 controls randomly selected from the population.]. 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:17768178;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP628002.RA2xscDDIHJdXmJP65qsOhBMUOMLU3__G-YLYhz0n3mvo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:30+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}