@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP498098.RAAUp87xmR6gh2QsIPNx9SgJ3ZBzyK-xBlT2oRZcWgudo> .
@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#> .
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  this: np:hasAssertion dgn-np:NP498098.RAAUp87xmR6gh2QsIPNx9SgJ3ZBzyK-xBlT2oRZcWgudo130_assertion ;
    np:hasProvenance dgn-np:NP498098.RAAUp87xmR6gh2QsIPNx9SgJ3ZBzyK-xBlT2oRZcWgudo130_provenance ;
    np:hasPublicationInfo dgn-np:NP498098.RAAUp87xmR6gh2QsIPNx9SgJ3ZBzyK-xBlT2oRZcWgudo130_publicationInfo ;
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  dgn-np:NP498098.RAAUp87xmR6gh2QsIPNx9SgJ3ZBzyK-xBlT2oRZcWgudo130_provenance a np:Provenance .
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}
dgn-np:NP498098.RAAUp87xmR6gh2QsIPNx9SgJ3ZBzyK-xBlT2oRZcWgudo130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  lld:C0023452 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP498098.RAAUp87xmR6gh2QsIPNx9SgJ3ZBzyK-xBlT2oRZcWgudo130_provenance {
  dgn-np:NP498098.RAAUp87xmR6gh2QsIPNx9SgJ3ZBzyK-xBlT2oRZcWgudo130_assertion dcterms:description "[The patterns and frequencies of lesions detected in the adult samples largely reproduced known genomic hallmarks detected in previous single nucleotide polymorphism-array studies of pediatric acute lymphoblastic leukemia, such as common deletions of 3p14.2 (FHIT), 5q33.3 (EBF), 6q, 9p21.3 (CDKN2A/B), 9p13.2 (PAX5), 13q14.2 (RB1) and 17q11.2 (NF1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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}
dgn-np:NP498098.RAAUp87xmR6gh2QsIPNx9SgJ3ZBzyK-xBlT2oRZcWgudo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:57+02:00"^^xsd:dateTime ;
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    dcterms:rightsHolder dgn-void:IBIGroup ;
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}