@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg> .
@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 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:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_head {
  this: np:hasAssertion dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_assertion;
    np:hasProvenance dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_provenance;
    np:hasPublicationInfo dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_assertion a np:Assertion .
  
  dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_provenance a np:Provenance .
  
  dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_assertion {
  miriam-gene:4536 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN16f0f9039c49d944c964c4b39b2bf080 sio:SIO_000628 miriam-gene:4536, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_provenance {
  dgn-np:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_assertion dct:description
      "[After applying three Cox proportional hazard models adjusted for American Joint Committee on Cancer (AJCC) stage, age and sex, three single nucleotide polymorphisms, two located in the 12S ribosomal RNA region (G752A and G1440A) and one in the nicotinamide adenine dinucleotide dehydrogenase subunit 2 region (ND2) region (G4770A), were statistically significantly associated with all-cause (Model I P-values: 0.0001, 0.002 and 0.002, respectively) and CRC-specific mortality (Model I P-values: 5 x 10(-5), 0.0003 and 0.0006, respectively).]. 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:19945968;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP70901.RAZiYD2WRNfW7neJh5WO7KGYj8_MpLcS-KtcupBDsQ4Jg130_publicationInfo {
  this: dct:created "2014-10-02T12:32:34+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}