@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g> .
@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:NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g130_head {
  this: np:hasAssertion dgn-np:NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g130_assertion;
    np:hasProvenance dgn-np:NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g130_provenance;
    np:hasPublicationInfo dgn-np:NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g130_assertion a np:Assertion .
  
  dgn-np:NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g130_provenance a np:Provenance .
  
  dgn-np:NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0079744 a ncit:C7057 .
  
  dgn-gda:DGN4d9362f3099e3791c8f84233027e1766 sio:SIO_000628 miriam-gene:1029, lld:C0079744;
    a sio:SIO_001121 .
}

dgn-np:NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g130_provenance {
  dgn-np:NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g130_assertion dcterms:description
      "[Sequential samples of the indolent and transformed phase of three cases showed the presence of p16(INK4a) deletions in the Richter's syndrome but not in the CLL component of two cases, whereas in a follicular lymphoma the deletion was present in both the follicular tumor and in the diffuse large-cell lymphoma.]. 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:9531609;
    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:NP1392329.RA1FLDknshk5sFmEfplg3VB1T9D-2-ue5qrcoAnd6qw4g130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:17+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" .
}