@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1249744.RA4OEvIBDOn6qOoSPJRf7YxvQg5AhnklVLaLLyt0R5dGA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1249744.RA4OEvIBDOn6qOoSPJRf7YxvQg5AhnklVLaLLyt0R5dGA130_head {
   this: np:hasAssertion dgn-np:NP1249744.RA4OEvIBDOn6qOoSPJRf7YxvQg5AhnklVLaLLyt0R5dGA130_assertion ;
    np:hasProvenance dgn-np:NP1249744.RA4OEvIBDOn6qOoSPJRf7YxvQg5AhnklVLaLLyt0R5dGA130_provenance ;
    np:hasPublicationInfo dgn-np:NP1249744.RA4OEvIBDOn6qOoSPJRf7YxvQg5AhnklVLaLLyt0R5dGA130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP1249744.RA4OEvIBDOn6qOoSPJRf7YxvQg5AhnklVLaLLyt0R5dGA130_provenance a np:Provenance .
  dgn-np:NP1249744.RA4OEvIBDOn6qOoSPJRf7YxvQg5AhnklVLaLLyt0R5dGA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1249744.RA4OEvIBDOn6qOoSPJRf7YxvQg5AhnklVLaLLyt0R5dGA130_assertion {
   miriam-gene:9967 a ncit:C16612 .
  lld:C2239176 a ncit:C7057 .
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}
dgn-np:NP1249744.RA4OEvIBDOn6qOoSPJRf7YxvQg5AhnklVLaLLyt0R5dGA130_provenance {
   dgn-np:NP1249744.RA4OEvIBDOn6qOoSPJRf7YxvQg5AhnklVLaLLyt0R5dGA130_assertion dcterms:description "[Furthermore, by taking account of genomic mutations causing transcriptional aberrations, we could improve the sensitivity of deleterious mutation detection in known cancer driver genes (TP53, AXIN1, ARID2, RPS6KA3), and identified recurrent disruptions in putative cancer driver genes such as HNF4A, CPS1, TSC1 and THRAP3 in HCCs.]. 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:25526364 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1249744.RA4OEvIBDOn6qOoSPJRf7YxvQg5AhnklVLaLLyt0R5dGA130_publicationInfo {
   this: dcterms:created "2016-05-13T12:51:12+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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> ;
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}