@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k> .
@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 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:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_head {
  this: np:hasAssertion dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_assertion;
    np:hasProvenance dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_provenance;
    np:hasPublicationInfo dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_assertion a np:Assertion .
  
  dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_provenance a np:Provenance .
  
  dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_assertion {
  miriam-gene:2067 a ncit:C16612 .
  
  lld:C0919267 a ncit:C7057 .
  
  dgn-gda:DGN9e59980703953c08ece343f6c9686aac sio:SIO_000628 miriam-gene:2067, lld:C0919267;
    a sio:SIO_001122 .
}

dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_provenance {
  dgn-np:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_assertion dc:description
      "[Although the ERCC1 codon 118 polymorphism does not seem to be associated with clinical outcome, the C8092A polymorphism was an independent predictor of survivalin women with optimally resected stage III epithelial ovarian 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:18640939;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP126152.RAlaJpaaOkP2cBRUypu1cmHXE4pnzU_938dsvrMo4mH7k130_publicationInfo {
  this: dc:created "2014-10-02T12:33:05+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}