@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg130_head {
  this: np:hasAssertion dgn-np:NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg130_assertion;
    np:hasProvenance dgn-np:NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg130_provenance;
    np:hasPublicationInfo dgn-np:NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg130_assertion a np:Assertion .
  
  dgn-np:NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg130_provenance a np:Provenance .
  
  dgn-np:NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg130_assertion {
  miriam-gene:2068 a ncit:C16612 .
  
  lld:C0546837 a ncit:C7057 .
  
  dgn-gda:DGN8e25bf98743f0352fd6937a7343dc053 sio:SIO_000628 miriam-gene:2068, lld:C0546837;
    a sio:SIO_001122 .
}

dgn-np:NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg130_provenance {
  dgn-np:NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg130_assertion dcterms:description
      "[Genetic variants in ERCC2 and ERCC4 may provide further survival prediction in addition to TNM staging system of esophageal cancer, which is more evident in the patients with early disease status.]. 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:21490450;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP382088.RAThQnKnyeP_15BbNkNbqX9nP8irrfitxC0K7HeUnCjqg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:21+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}