@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP863669.RALdcjFhIy2HL5WNRMcGY24-_ITZQd6ZSGIIaWnlzkaHY> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP863669.RALdcjFhIy2HL5WNRMcGY24-_ITZQd6ZSGIIaWnlzkaHY130_head {
   this: np:hasAssertion dgn-np:NP863669.RALdcjFhIy2HL5WNRMcGY24-_ITZQd6ZSGIIaWnlzkaHY130_assertion ;
    np:hasProvenance dgn-np:NP863669.RALdcjFhIy2HL5WNRMcGY24-_ITZQd6ZSGIIaWnlzkaHY130_provenance ;
    np:hasPublicationInfo dgn-np:NP863669.RALdcjFhIy2HL5WNRMcGY24-_ITZQd6ZSGIIaWnlzkaHY130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP863669.RALdcjFhIy2HL5WNRMcGY24-_ITZQd6ZSGIIaWnlzkaHY130_provenance a np:Provenance .
  dgn-np:NP863669.RALdcjFhIy2HL5WNRMcGY24-_ITZQd6ZSGIIaWnlzkaHY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP863669.RALdcjFhIy2HL5WNRMcGY24-_ITZQd6ZSGIIaWnlzkaHY130_assertion {
   miriam-gene:11277 a ncit:C16612 .
  lld:C0027627 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP863669.RALdcjFhIy2HL5WNRMcGY24-_ITZQd6ZSGIIaWnlzkaHY130_provenance {
   dgn-np:NP863669.RALdcjFhIy2HL5WNRMcGY24-_ITZQd6ZSGIIaWnlzkaHY130_assertion dcterms:description "[At a false discovery rate of 1% (p ≤ .0015), 15 SNPs of EXO1, MLH1, MSH2, MSH3, MSH6, PMS2, PMS2L3, TP73, and TREX1 in patients with localized disease (n = 333) and 6 SNPs of MSH3, MSH6, and TP73 in patients with locally advanced or metastatic disease (n = 373) were significantly associated with OS.]. 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:21212431 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
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  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP863669.RALdcjFhIy2HL5WNRMcGY24-_ITZQd6ZSGIIaWnlzkaHY130_publicationInfo {
   this: dcterms:created "2016-05-13T12:48:16+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}