@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI> .
@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:NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI130_head {
  this: np:hasAssertion dgn-np:NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI130_assertion;
    np:hasProvenance dgn-np:NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI130_provenance;
    np:hasPublicationInfo dgn-np:NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI130_assertion a np:Assertion .
  
  dgn-np:NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI130_provenance a np:Provenance .
  
  dgn-np:NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI130_assertion {
  miriam-gene:4521 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNef183bd72970eb77611226d745e9cc07 sio:SIO_000628 miriam-gene:4521, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI130_provenance {
  dgn-np:NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI130_assertion dcterms:description
      "[These data provide the strongest evidence to date for a causative role of BER defects in colorectal cancer etiology and show, to our knowledge for the first time, that heterozygous MUTYH mutations predispose to colorectal cancer later in life. These findings have clinical relevance for BER gene testing for patients with colorectal cancer and for genetic counseling of their relatives.]. 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:15931596;
    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:NP53548.RAVAJAABmSxtfBg8W8mbEZ5SSoj1d5zwm1pN33Zwb-irI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}