@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM> .
@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:NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM130_head {
  this: np:hasAssertion dgn-np:NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM130_assertion;
    np:hasProvenance dgn-np:NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM130_provenance;
    np:hasPublicationInfo dgn-np:NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM130_assertion a np:Assertion .
  
  dgn-np:NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM130_provenance a np:Provenance .
  
  dgn-np:NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM130_assertion {
  miriam-gene:2122 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGNc4323ed21eb510508848d04b0e6303ec sio:SIO_000628 miriam-gene:2122, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM130_provenance {
  dgn-np:NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM130_assertion dcterms:description
      "[These results suggest that EVI1 overexpression was the major factor contributing to leukemogenesis, and the late appearance of the Ph chromosome is closely associated with the progression to an aggressive form of 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:18206536;
    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:NP239613.RATFEQQUN6_ZZtHxuERhFgmVEaJ4UGHfwNKHzqPXUM9OM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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" .
}