@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE> .
@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:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_head {
  this: np:hasAssertion dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_assertion ;
    np:hasProvenance dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_provenance ;
    np:hasPublicationInfo dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_assertion a np:Assertion .
  dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_provenance a np:Provenance .
  dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_assertion {
  miriam-gene:2241 a ncit:C16612 .
  lld:C0023467 a ncit:C7057 .
  dgn-gda:DGNda9648f62df1c12e0c768e2b5831be12 sio:SIO_000628 miriam-gene:2241 , lld:C0023467 ;
    a sio:SIO_001121 .
}
dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_provenance {
  dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_assertion dcterms:description "[In this study, we analysed the prognostic relevance of foetal liver tyrosine kinase 3 (FLT3) mutations in 73 patients with acute myeloid leukaemia (AML) with normal karyotype, who survived induction and consolidation and received autologous stem cell transplantation (ASCT) after successful mobilization of peripheral blood stem cell (PBSC).]. 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:17036374 ;
    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:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:52+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" .
}