@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4> .
@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:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_head {
  this: np:hasAssertion dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_assertion;
    np:hasProvenance dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_provenance;
    np:hasPublicationInfo dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_assertion a np:Assertion .
  
  dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_provenance a np:Provenance .
  
  dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0349631 a ncit:C7057 .
  
  dgn-gda:DGNa39077c3995b67d59439b2caef089e0f sio:SIO_000628 miriam-gene:1029, lld:C0349631;
    a sio:SIO_001121 .
}

dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_provenance {
  dgn-np:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_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-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:NP902729.RA0djCb24S1srN0MHWclRGZFiKEogf1flyeZ7X4IdUqu4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:14+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" .
}