@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg> .
@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:NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg130_head {
  this: np:hasAssertion dgn-np:NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg130_assertion;
    np:hasProvenance dgn-np:NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg130_provenance;
    np:hasPublicationInfo dgn-np:NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg130_assertion a np:Assertion .
  
  dgn-np:NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg130_provenance a np:Provenance .
  
  dgn-np:NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg130_assertion {
  miriam-gene:55247 a ncit:C16612 .
  
  lld:C1302401 a ncit:C7057 .
  
  dgn-gda:DGN649e77bcc67786a1106bf8ad4764e0ca sio:SIO_000628 miriam-gene:55247, lld:C1302401;
    a sio:SIO_001121 .
}

dgn-np:NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg130_provenance {
  dgn-np:NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg130_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:NP351746.RAOPFkwRKp-PooeuxyDPt5dC055KFyFSXDuk9jcz5pKMg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:26+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" .
}