@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ> .
@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 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:NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_head {
  this: np:hasAssertion dgn-np:NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_assertion;
    np:hasProvenance dgn-np:NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_provenance;
    np:hasPublicationInfo dgn-np:NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_assertion a np:Assertion .
  
  dgn-np:NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_provenance a np:Provenance .
  
  dgn-np:NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_assertion {
  miriam-gene:2068 a ncit:C16612 .
  
  lld:C0546837 a ncit:C7057 .
  
  dgn-gda:DGNe3bf30bb7f2ef8428dd7b450de5c78be sio:SIO_000628 miriam-gene:2068, lld:C0546837;
    a sio:SIO_001122 .
}

dgn-np:NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_provenance {
  dgn-np:NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_assertion dct:description
      "[We conclude that  the malignant phenotype probably results from a summation of polymorphic nucleotide excision repair genes showing opposing effects (an increased risk of XPC versus a protective effect of XPD). The protective effect of the homozygous variant of XRCC1 Arg399Gln for GERD and BE suggests that base excision repair alterations may occur early in progression to EADC, likely in response to GERD-induced endogenous oxidative or inflammatory DNA damage. As GERD and BE are highly prevalent in the general population, this protective effect may well explain why only a fraction of individuals with GERD and BE progress into invasive EADC.]. 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:15878910;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP44864.RAkEH9np-LYnW0scWEMBgAN9wadEqFikAWDJsY5xW0weQ130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}