@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP227809.RAvDNhtMLAUBUjlpw9f9qwqu_zP7j7eBLNpy2ivIucWF4> .
@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:NP227809.RAvDNhtMLAUBUjlpw9f9qwqu_zP7j7eBLNpy2ivIucWF4130_head {
  this: np:hasAssertion dgn-np:NP227809.RAvDNhtMLAUBUjlpw9f9qwqu_zP7j7eBLNpy2ivIucWF4130_assertion;
    np:hasProvenance dgn-np:NP227809.RAvDNhtMLAUBUjlpw9f9qwqu_zP7j7eBLNpy2ivIucWF4130_provenance;
    np:hasPublicationInfo dgn-np:NP227809.RAvDNhtMLAUBUjlpw9f9qwqu_zP7j7eBLNpy2ivIucWF4130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP227809.RAvDNhtMLAUBUjlpw9f9qwqu_zP7j7eBLNpy2ivIucWF4130_provenance a np:Provenance .
  
  dgn-np:NP227809.RAvDNhtMLAUBUjlpw9f9qwqu_zP7j7eBLNpy2ivIucWF4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP227809.RAvDNhtMLAUBUjlpw9f9qwqu_zP7j7eBLNpy2ivIucWF4130_assertion {
  miriam-gene:4595 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
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dgn-np:NP227809.RAvDNhtMLAUBUjlpw9f9qwqu_zP7j7eBLNpy2ivIucWF4130_provenance {
  dgn-np:NP227809.RAvDNhtMLAUBUjlpw9f9qwqu_zP7j7eBLNpy2ivIucWF4130_assertion dcterms:description
      "[This article reviews the role of defective base excision repair, and MUTYH specifically, in colorectal cancer etiology and discusses the consequences of MUTYH gene defects, with particular emphasis on clinical relevance to colorectal polyposis, colorectal cancer risk, and appraising the risk of extra-colonic malignancy.]. 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:19793568;
    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:NP227809.RAvDNhtMLAUBUjlpw9f9qwqu_zP7j7eBLNpy2ivIucWF4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:06+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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