@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM> .
@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 dcterms: <http://purl.org/dc/terms/> .
@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:NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM130_head {
  this: np:hasAssertion dgn-np:NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM130_assertion;
    np:hasProvenance dgn-np:NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM130_provenance;
    np:hasPublicationInfo dgn-np:NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM130_assertion a np:Assertion .
  
  dgn-np:NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM130_provenance a np:Provenance .
  
  dgn-np:NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM130_assertion {
  miriam-gene:2322 a ncit:C16612 .
  
  lld:C0027708 a ncit:C7057 .
  
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dgn-np:NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM130_provenance {
  dgn-np:NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM130_assertion dcterms:description
      "[We reviewed the frequency and prognostic significance of FLT3 (fms-like tyrosine kinase receptor-3) and NPM (nucleophosmin) gene mutations and WT1 (Wilms' tumor) and BAALC (brain and acute leukemia, cytoplasmic) gene expression in 100 consecutive patients with intermediate and poor cytogenetic risk de novo acute myeloid leukemia (AML) receiving conventional anthracycline-AraC based therapy.]. 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-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
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dgn-np:NP182098.RAtUj5ZO9x1VHPJQ2_v0pBecg51KCCE8IVE0_JJl2ZzhM130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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    prv:usedData dgn-void:disgenetrdf;
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