@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP925413.RA58K9A30E0gwVSUZ5JzVHK1LOWMUbL94OGmqPSMgWwt4> .
@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/v3.0.0/void/> .
dgn-np:NP925413.RA58K9A30E0gwVSUZ5JzVHK1LOWMUbL94OGmqPSMgWwt4130_head {
  this: np:hasAssertion dgn-np:NP925413.RA58K9A30E0gwVSUZ5JzVHK1LOWMUbL94OGmqPSMgWwt4130_assertion ;
    np:hasProvenance dgn-np:NP925413.RA58K9A30E0gwVSUZ5JzVHK1LOWMUbL94OGmqPSMgWwt4130_provenance ;
    np:hasPublicationInfo dgn-np:NP925413.RA58K9A30E0gwVSUZ5JzVHK1LOWMUbL94OGmqPSMgWwt4130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP925413.RA58K9A30E0gwVSUZ5JzVHK1LOWMUbL94OGmqPSMgWwt4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP925413.RA58K9A30E0gwVSUZ5JzVHK1LOWMUbL94OGmqPSMgWwt4130_assertion {
  miriam-gene:56955 a ncit:C16612 .
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dgn-np:NP925413.RA58K9A30E0gwVSUZ5JzVHK1LOWMUbL94OGmqPSMgWwt4130_provenance {
  dgn-np:NP925413.RA58K9A30E0gwVSUZ5JzVHK1LOWMUbL94OGmqPSMgWwt4130_assertion dcterms:description "[We performed exome sequencing and SNP array analysis of 45 ACCs and identified recurrent alterations in known driver genes (CTNNB1, TP53, CDKN2A, RB1 and MEN1) and in genes not previously reported in ACC (ZNRF3, DAXX, TERT and MED12), which we validated in an independent cohort of 77 ACCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20150227 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP925413.RA58K9A30E0gwVSUZ5JzVHK1LOWMUbL94OGmqPSMgWwt4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:05+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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