@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o> .
@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:NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o130_head {
  this: np:hasAssertion dgn-np:NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o130_assertion;
    np:hasProvenance dgn-np:NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o130_provenance;
    np:hasPublicationInfo dgn-np:NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o130_assertion a np:Assertion .
  
  dgn-np:NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o130_provenance a np:Provenance .
  
  dgn-np:NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o130_assertion {
  miriam-gene:4869 a ncit:C16612 .
  
  lld:C0598766 a ncit:C7057 .
  
  dgn-gda:DGN3bd4c595cd24c778d336dc473f4b5538 sio:SIO_000628 miriam-gene:4869, lld:C0598766;
    a sio:SIO_001121 .
}

dgn-np:NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o130_provenance {
  dgn-np:NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o130_assertion dcterms:description
      "[To evaluate the prognostic significance of CEBPA mutations in the context of established molecular markers in cytogenetically normal (CN) acute myeloid leukemia (AML) and gain biologic insights into leukemogenesis of the CN-AML molecular high-risk subset (FLT3 internal tandem duplication [ITD] positive and/or NPM1 wild type) that has a significantly higher incidence of CEBPA mutations than the molecular low-risk subset (FLT3-ITD negative and NPM1 mutated).]. 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:18809607;
    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:NP694430.RA9P2sXoSqfUF7Hl5ONxRjHvIx90aRaPZehxR-dz3SQ8o130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:00+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" .
}