@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI> .
@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:NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI130_head {
  this: np:hasAssertion dgn-np:NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI130_assertion;
    np:hasProvenance dgn-np:NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI130_provenance;
    np:hasPublicationInfo dgn-np:NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI130_assertion a np:Assertion .
  
  dgn-np:NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI130_provenance a np:Provenance .
  
  dgn-np:NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI130_assertion {
  miriam-gene:4968 a ncit:C16612 .
  
  lld:C0007103 a ncit:C7057 .
  
  dgn-gda:DGNba121acd51b810dc93954acda445ca94 sio:SIO_000628 miriam-gene:4968, lld:C0007103;
    a sio:SIO_001121 .
}

dgn-np:NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI130_provenance {
  dgn-np:NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI130_assertion dcterms:description
      "[The purpose of this study was to determine whether the human APEX and OGG1 genes, encoding proteins important in base excision repair (BER) of DNA, contain nucleotide sequence polymorphisms or are mutated somatically in tumors from women diagnosed with ovarian or endometrial cancer.]. 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:11465542;
    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:NP653620.RAsc9wmvo5uzLFQMWs5ChXNMwraJ4bB0AQsk-AGkAJFdI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:33+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" .
}