@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_head {
   this: np:hasAssertion dgn-np:NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_assertion ;
    np:hasProvenance dgn-np:NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_provenance ;
    np:hasPublicationInfo dgn-np:NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_assertion a np:Assertion .
  dgn-np:NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_provenance a np:Provenance .
  dgn-np:NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_assertion {
   miriam-gene:1050 a ncit:C16612 .
  lld:C0023470 a ncit:C7057 .
  dgn-gda:DGNec6ba926a54e2ce3efde1189841d1f75 sio:SIO_000628 miriam-gene:1050 , lld:C0023470 ;
    a sio:SIO_001122 .
}
dgn-np:NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_provenance {
   dgn-np:NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_assertion dct:description "[Systematic analysis of CEBPA mutations, in addition to that of alterations in master genes of hematopoiesis, may be useful to assess the prognosis of AML particularly in patients belonging to the 'intermediate' prognostic subgroup.]. 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:15674366 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP46979.RAvckrbQuRMrpfCED_SO9cWnCHrGZFjEQuUKyJc8ttJjM130_publicationInfo {
   this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}