@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g> .
@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:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_head {
  this: np:hasAssertion dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_assertion;
    np:hasProvenance dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_provenance;
    np:hasPublicationInfo dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_assertion a np:Assertion .
  
  dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_provenance a np:Provenance .
  
  dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  
  lld:C0017168 a ncit:C7057 .
  
  dgn-gda:DGNcddbc8f34fd5c5fb5452bf8bb11cda65 sio:SIO_000628 miriam-gene:7515, lld:C0017168;
    a sio:SIO_001121 .
}

dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_provenance {
  dgn-np:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_assertion dcterms:description
      "[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.]. 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: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:NP705196.RAr6nGqxS6WsWfhgwFyerzzebzJVsBVsqpJoTTtCX265g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}