@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ> .
@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:NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ130_head {
  this: np:hasAssertion dgn-np:NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ130_assertion;
    np:hasProvenance dgn-np:NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ130_provenance;
    np:hasPublicationInfo dgn-np:NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ130_assertion a np:Assertion .
  
  dgn-np:NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ130_provenance a np:Provenance .
  
  dgn-np:NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ130_assertion {
  miriam-gene:861 a ncit:C16612 .
  
  lld:C0023449 a ncit:C7057 .
  
  dgn-gda:DGN352613ada1212ef048c6143014f4ac03 sio:SIO_000628 miriam-gene:861, lld:C0023449;
    a sio:SIO_001121 .
}

dgn-np:NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ130_provenance {
  dgn-np:NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ130_assertion dcterms:description
      "[To understand the cytogenetic mechanisms responsible for multiple RUNX1 gene copy numbers in hematologic malignancies, we analyzed the chromosomal and molecular cytogenetic findings in bone marrow or peripheral blood samples of individuals who were diagnosed with acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), or 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:19167608;
    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:NP716295.RAZzmGj6kfKMlfYQyElCFBICBji2eyZueAOWqe6iAW9HQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:10+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: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" .
}