@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k> .
@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:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_head {
  this: np:hasAssertion dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_assertion;
    np:hasProvenance dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_provenance;
    np:hasPublicationInfo dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_assertion a np:Assertion .
  
  dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_provenance a np:Provenance .
  
  dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN5836c85b780907df47ebb67139c1a9ce sio:SIO_000628 miriam-gene:7515, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_provenance {
  dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_assertion dcterms:description
      "[Our meta-analysis provides an evidence for the association between XRCC1 Arg399Gln polymorphism and colorectal cancer risk in Chinese population, and XRCC1 Arg399Gln variant genotypes contribute to increased risk of colorectal cancer in Chinese.]. 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:23712778;
    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:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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" .
}