@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc> .
@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:NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc130_head {
  this: np:hasAssertion dgn-np:NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc130_assertion;
    np:hasProvenance dgn-np:NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc130_provenance;
    np:hasPublicationInfo dgn-np:NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc130_assertion a np:Assertion .
  
  dgn-np:NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc130_provenance a np:Provenance .
  
  dgn-np:NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc130_assertion {
  miriam-gene:5915 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN1e447ee0f9cb904cd7cd85b277105d2a sio:SIO_000628 miriam-gene:5915, lld:C0376358;
    a sio:SIO_001121 .
}

dgn-np:NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc130_provenance {
  dgn-np:NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc130_assertion dcterms:description
      "[The aim of our study was to evaluate the diagnostic value of aberrant promoter hypermethylation of retinoic acid receptor β2 (RARβ2) gene in serum DNA samples from patients with the diagnosis of PCa and benign prostatic hyperplasia (BPH), as a new epigenetic biomarker in distinguishing between malignant and non-malignant lesions.]. 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:23294958;
    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:NP616632.RA0fssOM_1dFTOQnAG86Ka9LJ2NH98TzpMYmsfrdDtOWc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:12+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" .
}