@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI> .
@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:NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI130_head {
  this: np:hasAssertion dgn-np:NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI130_assertion;
    np:hasProvenance dgn-np:NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI130_provenance;
    np:hasPublicationInfo dgn-np:NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI130_assertion a np:Assertion .
  
  dgn-np:NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI130_provenance a np:Provenance .
  
  dgn-np:NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI130_assertion {
  miriam-gene:861 a ncit:C16612 .
  
  lld:C0002893 a ncit:C7057 .
  
  dgn-gda:DGNc1b445f98dfd80a2cea9f1e4b7cb6f3c sio:SIO_000628 miriam-gene:861, lld:C0002893;
    a sio:SIO_001121 .
}

dgn-np:NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI130_provenance {
  dgn-np:NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI130_assertion dcterms:description
      "[AML1/RUNX1 mutations have been reported frequently in myelodysplastic syndrome (MDS) patients, especially those diagnosed with refractory anemia with excess blast (RAEB), RAEB in transformation (RAEBt), or AML following MDS (these categories are defined as MDS/AML).]. 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:16467864;
    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:NP535244.RAR5gXjUd2EITfGfU2k-8r7Z6vDPo3DTadRAER5c8bEYI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:47+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" .
}