@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ> .
@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:NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ130_head {
  this: np:hasAssertion dgn-np:NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ130_assertion;
    np:hasProvenance dgn-np:NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ130_provenance;
    np:hasPublicationInfo dgn-np:NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ130_assertion a np:Assertion .
  
  dgn-np:NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ130_provenance a np:Provenance .
  
  dgn-np:NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ130_assertion {
  miriam-gene:6344 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN399602dfd06c13ebe0808363de7362cd sio:SIO_000628 miriam-gene:6344, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ130_provenance {
  dgn-np:NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ130_assertion dcterms:description
      "[Given that the number of hypermethylated loci at 2q14.2 likely affects the range of silenced flanking genes, high frequency of simultaneous hypermethylation of three CpG islands (EN1, SCTR, and INHBB) may have potential influence on specific characteristics of CIMP+ colorectal cancers.]. 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:18403637;
    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:NP928176.RAVoCCY9hkk8feZlBoetrTzihhFTO5vxC1rvX7eP5oGIQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:29+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" .
}