@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU> .
@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:NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU130_head {
  this: np:hasAssertion dgn-np:NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU130_assertion;
    np:hasProvenance dgn-np:NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU130_provenance;
    np:hasPublicationInfo dgn-np:NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU130_assertion a np:Assertion .
  
  dgn-np:NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU130_provenance a np:Provenance .
  
  dgn-np:NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU130_assertion {
  miriam-gene:2072 a ncit:C16612 .
  
  lld:C0546837 a ncit:C7057 .
  
  dgn-gda:DGN4f28fcf626c92caf3b91f3b06cdccad4 sio:SIO_000628 miriam-gene:2072, lld:C0546837;
    a sio:SIO_001122 .
}

dgn-np:NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU130_provenance {
  dgn-np:NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU130_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:NP382568.RA1dY0cPq6Eat8r6gWnUBuaSlfaHNEuDliPtf_pbXV8gU130_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" .
}