@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw> .
@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:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_head {
  this: np:hasAssertion dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_assertion;
    np:hasProvenance dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_provenance;
    np:hasPublicationInfo dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_assertion a np:Assertion .
  
  dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_provenance a np:Provenance .
  
  dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_assertion {
  miriam-gene:864 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNe61a2884c1197f4ad906758fb4fb346d sio:SIO_000628 miriam-gene:864, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_provenance {
  dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_assertion dcterms:description
      "[Epigenetic changes in the methylation of the RUNX3 proximal promoter, but not common genetic changes in RUNX3, have been associated with both changes in the gene expression and development of the cancer.]. 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:21523770;
    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:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+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" .
}