@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ> .
@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:NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ130_head {
  this: np:hasAssertion dgn-np:NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ130_assertion;
    np:hasProvenance dgn-np:NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ130_provenance;
    np:hasPublicationInfo dgn-np:NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ130_assertion a np:Assertion .
  
  dgn-np:NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ130_provenance a np:Provenance .
  
  dgn-np:NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ130_assertion {
  miriam-gene:1236 a ncit:C16612 .
  
  lld:C0220615 a ncit:C7057 .
  
  dgn-gda:DGN5a3da390bed5fdf151b7302b0ea3be35 sio:SIO_000628 miriam-gene:1236, lld:C0220615;
    a sio:SIO_001121 .
}

dgn-np:NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ130_provenance {
  dgn-np:NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ130_assertion dcterms:description
      "[In order to clarify relationship between these key actors in methylation mechanisms and their potential impact on patient outcomes, we analysed 195 de novo AML patients for the expression of DNMT3A, 3B (and its non-catalytic variant 3B(NC)) and their correlations with the outcome and the expression of other common prognostic genetic biomarkers (EVI1, NPM1, FLT3ITD/TKD and MLL) in adult 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:23251566;
    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:NP825641.RA_Mh2PJQfW6uo68hcTMmUyHeHisprAbSj1yNup7RkEkQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:25+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>;
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