@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60> .
@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:NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60130_head {
  this: np:hasAssertion dgn-np:NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60130_assertion;
    np:hasProvenance dgn-np:NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60130_provenance;
    np:hasPublicationInfo dgn-np:NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60130_assertion a np:Assertion .
  
  dgn-np:NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60130_provenance a np:Provenance .
  
  dgn-np:NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60130_assertion {
  miriam-gene:4968 a ncit:C16612 .
  
  lld:C1302401 a ncit:C7057 .
  
  dgn-gda:DGN075d07b42707c1f343417989edb84704 sio:SIO_000628 miriam-gene:4968, lld:C1302401;
    a sio:SIO_001121 .
}

dgn-np:NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60130_provenance {
  dgn-np:NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60130_assertion dcterms:description
      "[To assess the contribution of inherited variants in genes involved in base excision repair and oxidative DNA damage including MUTYH, OGG1, NEIL1, NEIL2, NEIL3, NUDT1 and NTH1 to the multiple colorectal adenoma phenotype.]. 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:18515411;
    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:NP808080.RAs1ZObD-5k08-IIitL9M-F3BpXTKMRzX8IvmDABX_J60130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:15+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" .
}