@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg> .
@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:NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg130_head {
  this: np:hasAssertion dgn-np:NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg130_assertion;
    np:hasProvenance dgn-np:NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg130_provenance;
    np:hasPublicationInfo dgn-np:NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg130_assertion a np:Assertion .
  
  dgn-np:NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg130_provenance a np:Provenance .
  
  dgn-np:NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg130_assertion {
  miriam-gene:861 a ncit:C16612 .
  
  lld:C0023473 a ncit:C7057 .
  
  dgn-gda:DGN6f561e26d8f74ffc6d157baef2e006ec sio:SIO_000628 miriam-gene:861, lld:C0023473;
    a sio:SIO_001121 .
}

dgn-np:NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg130_provenance {
  dgn-np:NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg130_assertion dcterms:description
      "[Observations for mutations of the Runt domain of the AML1 gene in bone marrow cells were made in 300 patients, including 131 with acute myeloid leukemia (AML), 94 with myelodysplastic syndrome (MDS), 28 with blast crisis chronic myeloid leukemia (CML), 3 with atypical CML, 41 with acute lymphoblastic leukemia (ALL), and 3 with essential thrombocythemia (ET).]. 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:11023523;
    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:NP197653.RAM4RDunvizSLCk0YGctZIieH9tgYeH9971hWRcp9yWgg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:49+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" .
}