@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o> .
@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:NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o130_head {
   this: np:hasAssertion dgn-np:NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o130_assertion ;
    np:hasProvenance dgn-np:NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o130_provenance ;
    np:hasPublicationInfo dgn-np:NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o130_assertion a np:Assertion .
  dgn-np:NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o130_provenance a np:Provenance .
  dgn-np:NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o130_assertion {
   miriam-gene:2068 a ncit:C16612 .
  lld:C0034885 a ncit:C7057 .
  dgn-gda:DGN033369bf0f5bd3c5b10aeeb0dd965a1b sio:SIO_000628 miriam-gene:2068 , lld:C0034885 ;
    a sio:SIO_001122 .
}
dgn-np:NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o130_provenance {
   dgn-np:NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o130_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 ;
    sio:SIO_000772 miriam-pubmed:20504250 ;
    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:NP87879.RAeeEaPRArxGJQvE0aWSu0mbaCLyGHl2VOyOxhYdMpw8o130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:43+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" .
}