@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM> .
@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:NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM130_head {
   this: np:hasAssertion dgn-np:NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM130_assertion ;
    np:hasProvenance dgn-np:NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM130_provenance ;
    np:hasPublicationInfo dgn-np:NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM130_assertion a np:Assertion .
  dgn-np:NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM130_provenance a np:Provenance .
  dgn-np:NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM130_assertion {
   miriam-gene:2187 a ncit:C16612 .
  lld:C0085669 a ncit:C7057 .
  dgn-gda:DGN8e3dd137119b6148924c84e6e9327fb3 sio:SIO_000628 miriam-gene:2187 , lld:C0085669 ;
    a sio:SIO_001121 .
}
dgn-np:NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM130_provenance {
   dgn-np:NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM130_assertion dcterms:description "[Six hundred and thirty unselected cases of acute leukemia, with complete data regarding age, karyotype (with breakpoints), and the diagnosis according to the FAB classification, were available in the literature and from our unpublished cases for comparing the incidence of chromosomal abnormalities involving the long arm of chromosome #11 among age groups in acute nonlymphocytic leukemia (ANLL) and acute lymphocytic leukemia (ALL).]. 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:6592035 ;
    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:NP493082.RAVv5Bqv_FPPoU2eEEUXTCasrbgoaGcBcVsLn1obk3UzM130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:54+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" .
}