@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI> .
@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:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_head {
  this: np:hasAssertion dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_assertion;
    np:hasProvenance dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_provenance;
    np:hasPublicationInfo dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_assertion a np:Assertion .
  
  dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_provenance a np:Provenance .
  
  dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_assertion {
  miriam-gene:4869 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGNffd0ed69bc2802dd579f769b331298bf sio:SIO_000628 miriam-gene:4869, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_provenance {
  dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_assertion dcterms:description
      "[Mutations of the WT1 gene have been reported as the most common abnormality after NPM1 and FLT3 gene mutations in acute myeloid leukemia (AML), while KIT mutations are predominantly found in core-binding factor (CBF) AMLs.]. 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:21504297;
    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:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:27+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" .
}