@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY> .
@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 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:NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_head {
  this: np:hasAssertion dgn-np:NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_assertion;
    np:hasProvenance dgn-np:NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_provenance;
    np:hasPublicationInfo dgn-np:NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_assertion a np:Assertion .
  
  dgn-np:NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_provenance a np:Provenance .
  
  dgn-np:NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_assertion {
  miriam-gene:2322 a ncit:C16612 .
  
  lld:C0023470 a ncit:C7057 .
  
  dgn-gda:DGN89344d278ad18861570efab5e4c11a0c sio:SIO_000628 miriam-gene:2322, lld:C0023470;
    a sio:SIO_001122 .
}

dgn-np:NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_provenance {
  dgn-np:NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_assertion dct:description
      "[We studied a series of 68 subjects diagnosed with childhood acute myeloid leukemia (AML) using conventional cytogenetics and fluorescence in situ hybridization (FISH), polymerase chain reaction (PCR) to analyze mutations in FLT3 and NPM1 genes, and/or array comparative genomic hybridization (CGH).]. 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:20001230;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}