@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA> .
@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:NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA130_head {
  this: np:hasAssertion dgn-np:NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA130_assertion ;
    np:hasProvenance dgn-np:NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA130_provenance ;
    np:hasPublicationInfo dgn-np:NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA130_assertion a np:Assertion .
  dgn-np:NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA130_provenance a np:Provenance .
  dgn-np:NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA130_assertion {
  miriam-gene:6520 a ncit:C16612 .
  lld:C1516669 a ncit:C7057 .
  dgn-gda:DGN3ab44f08108e327db2c695ce86013b25 sio:SIO_000628 miriam-gene:6520 , lld:C1516669 ;
    a sio:SIO_001121 .
}
dgn-np:NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA130_provenance {
  dgn-np:NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA130_assertion dcterms:description "[To better define the significance of clonal evolution (CE) including 14q32 translocations involving the immunoglobulin heavy chain gene (IGH) in chronic lymphocytic leukemia (CLL), 105 patients were analyzed sequentially by fluorescence in situ hybridization (FISH) with the following panel of probes: 13q14/D13S25, 11q22/ATM, 17p13/TP53, #12-centromere and 14q32/IGH break-apart probe.]. 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:21767243 ;
    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:NP851671.RAPuCAgsTf1paEvaRLXC0rdhspLPcAEjco0Fc9LISUUuA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:40+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" .
}