@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI130_head {
  this: np:hasAssertion dgn-np:NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI130_assertion;
    np:hasProvenance dgn-np:NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI130_provenance;
    np:hasPublicationInfo dgn-np:NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI130_assertion a np:Assertion .
  
  dgn-np:NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI130_provenance a np:Provenance .
  
  dgn-np:NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI130_assertion {
  miriam-gene:2322 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGN613d3acbe6e58abd234ccb764d626677 sio:SIO_000628 miriam-gene:2322, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI130_provenance {
  dgn-np:NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI130_assertion dcterms:description
      "[Activating FLT3 mutations are the most common genetic aberrations in acute myeloid leukemia (AML), resulting in the constitutive activation of this receptor tyrosine kinase (RTK), but such mutations are rarely found in acute lymphoblastic leukemia (ALL).]. 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:15044257;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP437117.RAepxmpMtRymDK_-MeyVss9ZoYILVFymlCzm_TPONCufI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:03+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}