@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM> .
@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:NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_head {
  this: np:hasAssertion dgn-np:NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_assertion;
    np:hasProvenance dgn-np:NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_provenance;
    np:hasPublicationInfo dgn-np:NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_assertion a np:Assertion .
  
  dgn-np:NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_provenance a np:Provenance .
  
  dgn-np:NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGNeb4354413bde51d1e8dbe50bae068830 sio:SIO_000628 miriam-gene:7157, lld:C0023467;
    a sio:SIO_001122 .
}

dgn-np:NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_provenance {
  dgn-np:NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_assertion dcterms:description
      "[These point towards a variety of candidate genes that could contribute to the pathogenesis of minimally differentiated acute myeloid leukemia, including the tumor suppressor genes TP53 and NF1, and reinforced the importance of RUNX1 in this leukemia.]. 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:19773259;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP80247.RAtjtOB2OWUedrgs6jFXvkzzRChlLWndotQWUjyRCFeJM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:39+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" .
}