@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0> .
@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:NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0130_head {
  this: np:hasAssertion dgn-np:NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0130_assertion;
    np:hasProvenance dgn-np:NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0130_provenance;
    np:hasPublicationInfo dgn-np:NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0130_assertion a np:Assertion .
  
  dgn-np:NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0130_provenance a np:Provenance .
  
  dgn-np:NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0130_assertion {
  miriam-gene:1050 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGNf0f24dced15df9dc78d02a7f81d732bb sio:SIO_000628 miriam-gene:1050, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0130_provenance {
  dgn-np:NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0130_assertion dcterms:description
      "[Subtyping of acute myeloid leukemia requires an integration of information from the patient's clinical history (such as any prior preleukemic myeloid neoplasm or cytotoxic potentially leukemogenic therapy), the leukemia morphology, cytogenetic findings, and the mutation status of particular genes (NPM1, FLT3, and CEBPA).]. 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:23590662;
    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:NP1069812.RA59PP-8eNARPO-B_38ef2UHRpgJT0wB3w5q23wQxdmX0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:51+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" .
}