@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA> .
@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:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_head {
  this: np:hasAssertion dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_assertion ;
    np:hasProvenance dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_provenance ;
    np:hasPublicationInfo dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_assertion a np:Assertion .
  dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_provenance a np:Provenance .
  dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_assertion {
  miriam-gene:1050 a ncit:C16612 .
  lld:C2939461 a ncit:C7057 .
  dgn-gda:DGNc87e9df5c233f8a11a90a1ab8e84d5ff sio:SIO_000628 miriam-gene:1050 , lld:C2939461 ;
    a sio:SIO_001121 .
}
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_provenance {
  dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_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-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 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:38+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:disgenetrdf ;
    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 "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}