@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho> .
@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:NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho130_head {
  this: np:hasAssertion dgn-np:NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho130_assertion;
    np:hasProvenance dgn-np:NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho130_provenance;
    np:hasPublicationInfo dgn-np:NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho130_assertion a np:Assertion .
  
  dgn-np:NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho130_provenance a np:Provenance .
  
  dgn-np:NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C2239176 a ncit:C7057 .
  
  dgn-gda:DGN36b033866328ea6716cbd03ee88d0bc5 sio:SIO_000628 miriam-gene:1029, lld:C2239176;
    a sio:SIO_001121 .
}

dgn-np:NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho130_provenance {
  dgn-np:NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho130_assertion dcterms:description
      "[High-throughput short-read sequencing of exomes and whole cancer genomes in multiple human hepatocellular carcinoma (HCC) cohorts confirmed previously identified frequently mutated somatic genes, such as TP53, CTNNB1 and AXIN1, and identified several novel genes with moderate mutation frequencies, including ARID1A, ARID2, MLL, MLL2, MLL3, MLL4, IRF2, ATM, CDKN2A, FGF19, PIK3CA, RPS6KA3, JAK1, KEAP1, NFE2L2, C16orf62, LEPR, RAC2, and IL6ST.]. 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:24379610;
    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:NP1140867.RAaNX2cKOcRE68szidIIMrj0a3mPl7MpAIgawDkzcmdho130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:23+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}