@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY> .
@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:NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY130_head {
  this: np:hasAssertion dgn-np:NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY130_assertion;
    np:hasProvenance dgn-np:NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY130_provenance;
    np:hasPublicationInfo dgn-np:NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY130_assertion a np:Assertion .
  
  dgn-np:NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY130_provenance a np:Provenance .
  
  dgn-np:NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  
  lld:C0279626 a ncit:C7057 .
  
  dgn-gda:DGN2291f3586ec2876e313f0eb570119c82 sio:SIO_000628 miriam-gene:7515, lld:C0279626;
    a sio:SIO_001121 .
}

dgn-np:NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY130_provenance {
  dgn-np:NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY130_assertion dcterms:description
      "[To investigate the effect of XRCC1 genetic polymorphisms on codons 194, 280 and 399, we evaluated data from 105 patients of esophageal squamous cell carcinoma and 264 healthy controls, matching with age (+/-3 years), gender and ethnicity.]. 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:11400117;
    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:NP168081.RAn8MJepE2NXlHa3GMqCYV7PlzZ8lFQko_rbkDNFoU3zY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}