@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc> .
@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:NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc130_head {
  this: np:hasAssertion dgn-np:NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc130_assertion;
    np:hasProvenance dgn-np:NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc130_provenance;
    np:hasPublicationInfo dgn-np:NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc130_assertion a np:Assertion .
  
  dgn-np:NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc130_provenance a np:Provenance .
  
  dgn-np:NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc130_assertion {
  miriam-gene:2322 a ncit:C16612 .
  
  lld:C0023487 a ncit:C7057 .
  
  dgn-gda:DGN9f125a1efd0e402ee14472aac9c37f4e sio:SIO_000628 miriam-gene:2322, lld:C0023487;
    a sio:SIO_001121 .
}

dgn-np:NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc130_provenance {
  dgn-np:NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc130_assertion dcterms:description
      "[The authors examined internal tandem duplication (ITD) and Asp835 mutations of FLT3 in patients with acute promyelocytic leukemia (APL) to determine the incidence of these mutations and to analyze the results for correlations with clinicohematologic features and outcome.]. 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:12973844;
    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:NP232870.RAJmpD-Y1_jXIvWVncEGj0HXsn9GodRMF-2ZR4UMbC2uc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+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" .
}