@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP604568.RAag01yGYNOg0ZBhqqIm3BhJ6SnHdvjvsUzFAEupESjyM> .
@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:NP604568.RAag01yGYNOg0ZBhqqIm3BhJ6SnHdvjvsUzFAEupESjyM130_head {
  this: np:hasAssertion dgn-np:NP604568.RAag01yGYNOg0ZBhqqIm3BhJ6SnHdvjvsUzFAEupESjyM130_assertion ;
    np:hasProvenance dgn-np:NP604568.RAag01yGYNOg0ZBhqqIm3BhJ6SnHdvjvsUzFAEupESjyM130_provenance ;
    np:hasPublicationInfo dgn-np:NP604568.RAag01yGYNOg0ZBhqqIm3BhJ6SnHdvjvsUzFAEupESjyM130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP604568.RAag01yGYNOg0ZBhqqIm3BhJ6SnHdvjvsUzFAEupESjyM130_provenance a np:Provenance .
  dgn-np:NP604568.RAag01yGYNOg0ZBhqqIm3BhJ6SnHdvjvsUzFAEupESjyM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP604568.RAag01yGYNOg0ZBhqqIm3BhJ6SnHdvjvsUzFAEupESjyM130_assertion {
  miriam-gene:7508 a ncit:C16612 .
  lld:C1527249 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP604568.RAag01yGYNOg0ZBhqqIm3BhJ6SnHdvjvsUzFAEupESjyM130_provenance {
  dgn-np:NP604568.RAag01yGYNOg0ZBhqqIm3BhJ6SnHdvjvsUzFAEupESjyM130_assertion dcterms:description "[We observed a statistically significant interaction between the XPC Lys939Gln polymorphism and consumption of red meat, with a 3.7-fold increase in colorectal cancer risk per 100g red meat intake per day among carriers of the homozygous variant, but virtually no effect of red meat intake among carriers of the wild type allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP604568.RAag01yGYNOg0ZBhqqIm3BhJ6SnHdvjvsUzFAEupESjyM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:03+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}