@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4> .
@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:NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4130_head {
  this: np:hasAssertion dgn-np:NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4130_assertion ;
    np:hasProvenance dgn-np:NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4130_provenance ;
    np:hasPublicationInfo dgn-np:NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4130_assertion a np:Assertion .
  dgn-np:NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4130_provenance a np:Provenance .
  dgn-np:NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4130_assertion {
  miriam-gene:2526 a ncit:C16612 .
  lld:C0023467 a ncit:C7057 .
  dgn-gda:DGNf5f5d087d9c2af83aa6e77b36020659d sio:SIO_000628 miriam-gene:2526 , lld:C0023467 ;
    a sio:SIO_001121 .
}
dgn-np:NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4130_provenance {
  dgn-np:NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4130_assertion dcterms:description "[We investigated the genetic mutations NPM1, FLT3-ITD, and FLT3-TKD and expression of the membrane antigens CD7, CD15, CD34, and CD56 in 144 elderly patients with de novo normal karyotype acute myeloid leukemia to retrospectively analyze the prognostic and clinical relevance of these parameters.]. 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:22939316 ;
    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:NP487634.RA7dk_66nUXsngdVnAX3ATy2Y8E_RFSVB6f4xYwqNVTq4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:51+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: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" .
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}