@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4> .
@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:NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4130_head {
  this: np:hasAssertion dgn-np:NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4130_assertion;
    np:hasProvenance dgn-np:NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4130_provenance;
    np:hasPublicationInfo dgn-np:NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4130_assertion a np:Assertion .
  
  dgn-np:NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4130_provenance a np:Provenance .
  
  dgn-np:NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4130_assertion {
  miriam-gene:1666 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGN9d9fb1eedbb92c4732be06d9c26b4072 sio:SIO_000628 miriam-gene:1666, lld:C0242379;
    a sio:SIO_001121 .
}

dgn-np:NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4130_provenance {
  dgn-np:NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4130_assertion dcterms:description
      "[Epigenetic silencing of NADPH oxidases by hypermethylation of their promoter region or of the genes required for their assembly and activity occurs in diseases, such as lung cancer, and may represent an early stage of neoplastic transformation.]. 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:23126619;
    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:NP785066.RAQCAc-ez_DIzXtFyfedubHc7ifh9rj6QJzixDQarM4B4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:55+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" .
}