@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU> .
@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:NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU130_head {
  this: np:hasAssertion dgn-np:NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU130_assertion;
    np:hasProvenance dgn-np:NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU130_provenance;
    np:hasPublicationInfo dgn-np:NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU130_assertion a np:Assertion .
  
  dgn-np:NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU130_provenance a np:Provenance .
  
  dgn-np:NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU130_assertion {
  miriam-gene:131 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN6fc1c73df8feee1066de7316bb94a8ba sio:SIO_000628 miriam-gene:131, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU130_provenance {
  dgn-np:NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU130_assertion dcterms:description
      "[A nested case-control study (1269 cases matched to 2107 controls by sex, age, study centre and date of blood collection) was conducted within the European Prospective Investigation into Cancer and Nutrition (EPIC) to evaluate the impact of rs1229984 (ADH1B), rs1573496 (ADH7) and rs441 (ALDH2) polymorphisms on CRC risk.]. 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:23149980;
    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:NP332973.RAZoarEzF83ggBDii8u9VIDmN1P9_32UIH11GjXaCgGgU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:16+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" .
}