@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00> .
@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:NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00130_head {
  this: np:hasAssertion dgn-np:NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00130_assertion;
    np:hasProvenance dgn-np:NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00130_provenance;
    np:hasPublicationInfo dgn-np:NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00130_assertion a np:Assertion .
  
  dgn-np:NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00130_provenance a np:Provenance .
  
  dgn-np:NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C2239176 a ncit:C7057 .
  
  dgn-gda:DGN67d3975a3325ca0cc6288a819da809e3 sio:SIO_000628 miriam-gene:7157, lld:C2239176;
    a sio:SIO_001121 .
}

dgn-np:NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00130_provenance {
  dgn-np:NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00130_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:NP1140856.RAkbp4qmLTCUfLfWIojh3zCZs3x-XTgn43-0LQb0uXz00130_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" .
}