@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec> .
@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:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_head {
  this: np:hasAssertion dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_assertion;
    np:hasProvenance dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_provenance;
    np:hasPublicationInfo dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_assertion a np:Assertion .
  
  dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_provenance a np:Provenance .
  
  dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_assertion {
  miriam-gene:7507 a ncit:C16612 .
  
  lld:C1559154 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_provenance {
  dgn-np:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_assertion dcterms:description
      "[The hereditary genetic variants in XPA and XPC can serve as independent predictors of the clinical outcome of patients with ESCC, especially in those who are treated with esophagectomy and undergo chemoradiation.]. 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:22941172;
    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:NP484785.RAAkqAC6amTBDvSQ0bqqJNu83UEolJ3mc_70vkd77Ssec130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:50+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" .
}