@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI> .
@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:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_head {
  this: np:hasAssertion dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_assertion;
    np:hasProvenance dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_provenance;
    np:hasPublicationInfo dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_assertion a np:Assertion .
  
  dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_provenance a np:Provenance .
  
  dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_assertion {
  miriam-gene:7298 a ncit:C16612 .
  
  lld:C0021843 a ncit:C7057 .
  
  dgn-gda:DGN49fe38e6be5e745b943e2d396c5c110d sio:SIO_000628 miriam-gene:7298, lld:C0021843;
    a sio:SIO_001121 .
}

dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_provenance {
  dgn-np:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_assertion dcterms:description
      "[Cox multivariate analysis, adjusted for the prognostic impact of disease stage, vascular tumor invasion, and bowel obstruction at resection, revealed that high TYMS gene copy number was associated with significantly higher risk of recurrence (HR = 1.6; 95%CI 1.1-2.2; p = 0.02) and death (HR = 1.6; 95%CI 1.1-2.3; p = 0.01).]. 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:18607850;
    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:NP167176.RATKMwaUUX8KCc32dJu_81hCAxDyQA_vSkaM-wqFF4urI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:30+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" .
}