@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg> .
@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:NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg130_head {
  this: np:hasAssertion dgn-np:NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg130_assertion;
    np:hasProvenance dgn-np:NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg130_provenance;
    np:hasPublicationInfo dgn-np:NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg130_assertion a np:Assertion .
  
  dgn-np:NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg130_provenance a np:Provenance .
  
  dgn-np:NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg130_assertion {
  miriam-gene:100862695 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN2cb425b344a775798583fc51d97b3f64 sio:SIO_000628 miriam-gene:100862695,
      lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg130_provenance {
  dgn-np:NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg130_assertion dcterms:description
      "[Interestingly, the frequencies of 194Trp and 399Gln genotypes were higher in colorectal cancer cases under age 40 than in corresponding controls, and an association between both polymorphisms and early age of disease onset was observed (OR=3.33, 95% CL 0.48-35.90, and P=0.16 for 194Trp and OR=11.90, 95% CL 2.30-51.50, and P=0.0003 for 399Gln).]. 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:10974409;
    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:NP874755.RAFIIPekp9TEGKruXy-LTW0u9DafilOoehH82cqaF9ylg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:54+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" .
}