@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo> .
@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:NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo130_head {
  this: np:hasAssertion dgn-np:NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo130_assertion ;
    np:hasProvenance dgn-np:NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo130_provenance ;
    np:hasPublicationInfo dgn-np:NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo130_assertion a np:Assertion .
  dgn-np:NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo130_provenance a np:Provenance .
  dgn-np:NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo130_assertion {
  miriam-gene:7153 a ncit:C16612 .
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    a sio:SIO_001121 .
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dgn-np:NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo130_provenance {
  dgn-np:NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo130_assertion dcterms:description "[We sought to determine the potential role of genetic variants within the topoisomerase IIα gene (TOP2A), within the mixed lineage leukemia gene (MLL) and two of its translocation partners, cyclin AMP response element-binding protein gene (CREBBP) and E1A binding protein gene (EP300) in the increased sensitivity of Hispanic children with ALL to topo II inhibitors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP488379.RAKFTMWlwjlx0vV6XEruvXavPVKyRYtmlAniO2LL6VVJo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:52+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    pav:version "v2.1.0.0" .
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}