@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP498165.RAHiFVfBnaYdRYezoqu8axVIgCVia_LDLpO89dNjbHyms> .
@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:NP498165.RAHiFVfBnaYdRYezoqu8axVIgCVia_LDLpO89dNjbHyms130_head {
  this: np:hasAssertion dgn-np:NP498165.RAHiFVfBnaYdRYezoqu8axVIgCVia_LDLpO89dNjbHyms130_assertion;
    np:hasProvenance dgn-np:NP498165.RAHiFVfBnaYdRYezoqu8axVIgCVia_LDLpO89dNjbHyms130_provenance;
    np:hasPublicationInfo dgn-np:NP498165.RAHiFVfBnaYdRYezoqu8axVIgCVia_LDLpO89dNjbHyms130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP498165.RAHiFVfBnaYdRYezoqu8axVIgCVia_LDLpO89dNjbHyms130_assertion a np:Assertion .
  
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  dgn-np:NP498165.RAHiFVfBnaYdRYezoqu8axVIgCVia_LDLpO89dNjbHyms130_publicationInfo a
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}

dgn-np:NP498165.RAHiFVfBnaYdRYezoqu8axVIgCVia_LDLpO89dNjbHyms130_assertion {
  miriam-gene:4363 a ncit:C16612 .
  
  lld:C0085669 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP498165.RAHiFVfBnaYdRYezoqu8axVIgCVia_LDLpO89dNjbHyms130_provenance {
  dgn-np:NP498165.RAHiFVfBnaYdRYezoqu8axVIgCVia_LDLpO89dNjbHyms130_assertion dcterms:description
      "[In this study, we correlated the results of concurrent molecular and cytogenetic detection of entity-defining translocations in adults with acute leukemia to determine the frequency of cryptic translocations missed by conventional cytogenetics (CC) and of recurrent, prognostically relevant translocations not detectable by multiplex reverse transcriptase-polymerase chain reaction (MRP).]. 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;
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  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:NP498165.RAHiFVfBnaYdRYezoqu8axVIgCVia_LDLpO89dNjbHyms130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:57+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>,
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
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