@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4> .
@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:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_head {
  this: np:hasAssertion dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_assertion;
    np:hasProvenance dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_provenance;
    np:hasPublicationInfo dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_assertion a np:Assertion .
  
  dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_provenance a np:Provenance .
  
  dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_assertion {
  miriam-gene:864 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGNc1b1ef5a413f2362bc73981e4f1d47ff sio:SIO_000628 miriam-gene:864, lld:C0242379;
    a sio:SIO_001121 .
}

dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_provenance {
  dgn-np:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_assertion dcterms:description
      "[These results indicated that silencing of the RUNX3 gene plays an important role in the pathogenesis of lung cancer, and aberrant methylation is an important mechanism of inactivation of the RUNX3 gene in lung AdC.]. 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:16328045;
    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:NP578954.RA1BO21U9eiS7OkDI_NagcSZKQI4anCDoUhMyKtSpHyM4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:49+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" .
}