@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg> .
@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:NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg130_head {
  this: np:hasAssertion dgn-np:NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg130_assertion ;
    np:hasProvenance dgn-np:NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg130_provenance ;
    np:hasPublicationInfo dgn-np:NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg130_assertion a np:Assertion .
  dgn-np:NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg130_provenance a np:Provenance .
  dgn-np:NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg130_assertion {
  miriam-gene:4193 a ncit:C16612 .
  lld:C1527249 a ncit:C7057 .
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dgn-np:NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg130_provenance {
  dgn-np:NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg130_assertion dcterms:description "[ This study failed to show any role of the p53 polymorphism on age of colorectal cancer onset in Lynch syndrome and sporadic colorectal cancer. The polymorphism in the MDM2 promoter had no affect on age of onset in Lynch syndrome. Accurate information about age of onset is important in clinical practice, especially in high-risk conditions. As association studies are vulnerable to biologically insignificant variation, both positive and negative findings need to be reported to enable unbiased assessment of the significance of putative risk variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:gad-20130706 ;
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  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 ;
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dgn-np:NP62644.RAsCHa2axUnLE4zbFF_tHJImspXaUYaCuw6gTo6KK7Kxg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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