@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA130_head {
  this: np:hasAssertion dgn-np:NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA130_assertion;
    np:hasProvenance dgn-np:NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA130_provenance;
    np:hasPublicationInfo dgn-np:NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA130_assertion a np:Assertion .
  
  dgn-np:NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA130_provenance a np:Provenance .
  
  dgn-np:NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA130_assertion {
  miriam-gene:3492 a ncit:C16612 .
  
  lld:C0023434 a ncit:C7057 .
  
  dgn-gda:DGNc1e30cbfa933a715196ae557192d8259 sio:SIO_000628 miriam-gene:3492, lld:C0023434;
    a sio:SIO_001122 .
}

dgn-np:NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA130_provenance {
  dgn-np:NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA130_assertion dcterms:description
      "[We identified a novel t(10;14)(p12;q32)/IGH-BMI1 rearrangement and its IGL variant in six cases of chronic lymphocytic leukemia (CLL) and found that these aberrations were consistently acquired at time of disease progression and high grade transformation of leukemia (Richter syndrome).]. 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:23873701;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1095570.RA7SgyMOMzulDu1zkZ57f_DoPAGJKT7XJdm7sDeSFmwFA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:02+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}