@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg> .
@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:NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg130_head {
  this: np:hasAssertion dgn-np:NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg130_assertion;
    np:hasProvenance dgn-np:NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg130_provenance;
    np:hasPublicationInfo dgn-np:NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg130_assertion a np:Assertion .
  
  dgn-np:NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg130_provenance a np:Provenance .
  
  dgn-np:NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg130_assertion {
  miriam-gene:64921 a ncit:C16612 .
  
  lld:C0153439 a ncit:C7057 .
  
  dgn-gda:DGNff67019be07ad96864fe14ca92c59e9b sio:SIO_000628 miriam-gene:64921, lld:C0153439;
    a sio:SIO_001121 .
}

dgn-np:NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg130_provenance {
  dgn-np:NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg130_assertion dcterms:description
      "[To investigate whether this is reflected in differences in somatic mutation frequency in the background mucosa, mutation of the neutral O-acetyltransferase gene (oat) was quantified in histologically normal resection margins from 20 informative (heterozygous) patients with caecal or ascending colon cancer (11 males, median age 75 years) and 20 with sigmoid colon or rectal cancer (10 males, median age 70 years).]. 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:9875137;
    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:NP469277.RACC7FHaZKfNg2-TkZwfiu2oslQ7CcHMmgzcjlRAd1LCg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:41+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>;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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