@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw> .
@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:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_head {
  this: np:hasAssertion dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_assertion;
    np:hasProvenance dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_provenance;
    np:hasPublicationInfo dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_assertion a np:Assertion .
  
  dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_provenance a np:Provenance .
  
  dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_assertion {
  miriam-gene:7528 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN8e285b379d564f3a32683616cd3f06f5 sio:SIO_000628 miriam-gene:7528, lld:C0376358;
    a sio:SIO_001121 .
}

dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_provenance {
  dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_assertion dcterms:description
      "[In conclusion, we identified a new functional prostate cancer risk variant at the 8q24 locus, rs378854 allele G, that reduces binding of the YY1 protein and is associated with increased expression of PVT1 located 0.5 Mb downstream.]. 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:21814516;
    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:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:27+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" .
}