@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE130_head {
  this: np:hasAssertion dgn-np:NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE130_assertion;
    np:hasProvenance dgn-np:NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE130_provenance;
    np:hasPublicationInfo dgn-np:NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE130_assertion a np:Assertion .
  
  dgn-np:NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE130_provenance a np:Provenance .
  
  dgn-np:NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE130_assertion {
  miriam-gene:5371 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
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dgn-np:NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE130_provenance {
  dgn-np:NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE130_assertion dcterms:description
      "[Our analysis demonstrates that the single platform of gene expression profiling can accurately identify the known prognostically important genetic subtypes of ALL, including T-ALL, E2A-PBX1, TEL-AML1, MLL rearrangements, BCR-abl, and hyperdiploid &gt;50 chromosomes, and AML, including t(15;17)[PML-RARalpha], t(8;21)[AML1-ETO], inv(16)[CBFbeta-MYH11], MLL gene rearrangement, and cases with FAB-M7 morphology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
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}

dgn-np:NP562827.RABj1ZNKZstAU89EoesmVIk0dEykRZZ8DbfYlQhjayavE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:00+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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