@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0> .
@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:NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0130_head {
  this: np:hasAssertion dgn-np:NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0130_assertion ;
    np:hasProvenance dgn-np:NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0130_provenance ;
    np:hasPublicationInfo dgn-np:NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0130_assertion a np:Assertion .
  dgn-np:NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0130_provenance a np:Provenance .
  dgn-np:NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0130_assertion {
  miriam-gene:65059 a ncit:C16612 .
  lld:C0024305 a ncit:C7057 .
  dgn-gda:DGN00066a2b26e7f7adb7e60041d55fc934 sio:SIO_000628 miriam-gene:65059 , lld:C0024305 ;
    a sio:SIO_001121 .
}
dgn-np:NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0130_provenance {
  dgn-np:NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0130_assertion dcterms:description "[A total of 1652 attempts at cytogenetic analysis with banding technique were performed in 240 patients with acute nonlymphocytic leukaemia (ANLL), 177 with chronic myeloid leukaemia (CML), 157 with myelodysplasia (MDS), 82 with myeloproliferative disorders (MPD), 114 with acute lymphoblastic leukaemia (ALL), 42 with non-Hodgkin lymphoma or other lymphoproliferative disorders (NHL + LPD), and 120 patients with benign disorders.]. 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:3464085 ;
    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:NP696249.RAxLOORimuwKM8hj9uyfm75vyFG0HLOAszdtOrKxE45O0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:03+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" .
}