@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1248218.RA_f6_lC-cuMwzqjnwUiAJqoJhmWLbyF0I37evCIHVuCc> .
@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:NP1248218.RA_f6_lC-cuMwzqjnwUiAJqoJhmWLbyF0I37evCIHVuCc130_head {
  this: np:hasAssertion dgn-np:NP1248218.RA_f6_lC-cuMwzqjnwUiAJqoJhmWLbyF0I37evCIHVuCc130_assertion;
    np:hasProvenance dgn-np:NP1248218.RA_f6_lC-cuMwzqjnwUiAJqoJhmWLbyF0I37evCIHVuCc130_provenance;
    np:hasPublicationInfo dgn-np:NP1248218.RA_f6_lC-cuMwzqjnwUiAJqoJhmWLbyF0I37evCIHVuCc130_publicationInfo;
    a np:Nanopublication .
  
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    a np:PublicationInfo .
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dgn-np:NP1248218.RA_f6_lC-cuMwzqjnwUiAJqoJhmWLbyF0I37evCIHVuCc130_assertion {
  miriam-gene:2060 a ncit:C16612 .
  
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dgn-np:NP1248218.RA_f6_lC-cuMwzqjnwUiAJqoJhmWLbyF0I37evCIHVuCc130_provenance {
  dgn-np:NP1248218.RA_f6_lC-cuMwzqjnwUiAJqoJhmWLbyF0I37evCIHVuCc130_assertion dcterms:description
      "[Based on the large data collection of MLL genomic breakpoints in acute leukemias comprising more than 1.600 cases at the Diagnostic Center for Acute Leukemias (DCAL) in Frankfurt, Germany that provide an overview over the experimentally observed fusion transcript variants, we developed RT-PCR methods for the reliable detection of the 8 most common MLL aberrations (MLL-AF4, MLL-AF6, MLL-AF9, MLL-AF10, MLL-ENL, MLL-ELL, MLL-EPS15, MLL PTD), together accounting for around 90% of MLL-r cases.]. 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-2016;
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  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;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP1248218.RA_f6_lC-cuMwzqjnwUiAJqoJhmWLbyF0I37evCIHVuCc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:11+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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