@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M> .
@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:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_head {
  this: np:hasAssertion dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_assertion;
    np:hasProvenance dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_provenance;
    np:hasPublicationInfo dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_assertion a np:Assertion .
  
  dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_provenance a np:Provenance .
  
  dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_assertion {
  miriam-gene:1788 a ncit:C16612 .
  
  lld:C0023487 a ncit:C7057 .
  
  dgn-gda:DGN0d44ab8b5aeccd9abd4810f2bb23973c sio:SIO_000628 miriam-gene:1788, lld:C0023487;
    a sio:SIO_001121 .
}

dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_provenance {
  dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_assertion dcterms:description
      "[To assess their prognostic significance, we determined the mutational status of DNMT3A exon 23 in 288 patients with AML excluding acute promyelocytic leukemia, aged from 18 to 65 years and treated in Toulouse University Hospital.]. 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:22081665;
    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:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:55+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" .
}