@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP91420.RAdW78sLbxr1Hnr7Zb8NBVC74PJ8PNiFAc9hymeOTLSf4> .
@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:NP91420.RAdW78sLbxr1Hnr7Zb8NBVC74PJ8PNiFAc9hymeOTLSf4130_head {
   this: np:hasAssertion dgn-np:NP91420.RAdW78sLbxr1Hnr7Zb8NBVC74PJ8PNiFAc9hymeOTLSf4130_assertion ;
    np:hasProvenance dgn-np:NP91420.RAdW78sLbxr1Hnr7Zb8NBVC74PJ8PNiFAc9hymeOTLSf4130_provenance ;
    np:hasPublicationInfo dgn-np:NP91420.RAdW78sLbxr1Hnr7Zb8NBVC74PJ8PNiFAc9hymeOTLSf4130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP91420.RAdW78sLbxr1Hnr7Zb8NBVC74PJ8PNiFAc9hymeOTLSf4130_provenance a np:Provenance .
  dgn-np:NP91420.RAdW78sLbxr1Hnr7Zb8NBVC74PJ8PNiFAc9hymeOTLSf4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP91420.RAdW78sLbxr1Hnr7Zb8NBVC74PJ8PNiFAc9hymeOTLSf4130_assertion {
   miriam-gene:7515 a ncit:C16612 .
  lld:C0034885 a ncit:C7057 .
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    a sio:SIO_001122 .
}
dgn-np:NP91420.RAdW78sLbxr1Hnr7Zb8NBVC74PJ8PNiFAc9hymeOTLSf4130_provenance {
   dgn-np:NP91420.RAdW78sLbxr1Hnr7Zb8NBVC74PJ8PNiFAc9hymeOTLSf4130_assertion dcterms:description "[The detection of somatic mutations in rectal cancer tumors led us to re-evaluate the utility of the tests performed in blood samples for these polymorphisms in rectal cancer. Furthermore, studies aimed at assessing the influence of pharmacogenetic markers in treatment response performed in blood samples should take into account the particular pattern of hypermutability present in each tumor type. We hypothesize that different patterns of hypermutability present in each tumor type would be related to the different results in association studies related to response to the treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP91420.RAdW78sLbxr1Hnr7Zb8NBVC74PJ8PNiFAc9hymeOTLSf4130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:45+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}