@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1152104.RAz-Pil6DfAdYXkmH8xaY85Z9e4tWhYHi1mzKZ0z5cckQ130_head { this: np:hasAssertion dgn-np:NP1152104.RAz-Pil6DfAdYXkmH8xaY85Z9e4tWhYHi1mzKZ0z5cckQ130_assertion; np:hasProvenance dgn-np:NP1152104.RAz-Pil6DfAdYXkmH8xaY85Z9e4tWhYHi1mzKZ0z5cckQ130_provenance; np:hasPublicationInfo dgn-np:NP1152104.RAz-Pil6DfAdYXkmH8xaY85Z9e4tWhYHi1mzKZ0z5cckQ130_publicationInfo; a np:Nanopublication . dgn-np:NP1152104.RAz-Pil6DfAdYXkmH8xaY85Z9e4tWhYHi1mzKZ0z5cckQ130_assertion a np:Assertion . dgn-np:NP1152104.RAz-Pil6DfAdYXkmH8xaY85Z9e4tWhYHi1mzKZ0z5cckQ130_provenance a np:Provenance . dgn-np:NP1152104.RAz-Pil6DfAdYXkmH8xaY85Z9e4tWhYHi1mzKZ0z5cckQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP1152104.RAz-Pil6DfAdYXkmH8xaY85Z9e4tWhYHi1mzKZ0z5cckQ130_assertion { miriam-gene:596 a ncit:C16612 . lld:C0009447 a ncit:C7057 . dgn-gda:DGNd09d6b9118d1eabcfc3861faf8c1bb08 sio:SIO_000628 miriam-gene:596, lld:C0009447; a sio:SIO_001121 . } dgn-np:NP1152104.RAz-Pil6DfAdYXkmH8xaY85Z9e4tWhYHi1mzKZ0z5cckQ130_provenance { dgn-np:NP1152104.RAz-Pil6DfAdYXkmH8xaY85Z9e4tWhYHi1mzKZ0z5cckQ130_assertion dcterms:description "[By direct sequencing, we found clonally represented BCL2 mutations in 2/16 (13%) of t(14;18) negative FLs, 2/16 (13%) HIV-DLBCLs, 1/9 (11%) of Richter's syndrome DLBCL, 1/17 (6%) of post-transplant lymphoproliferative disorders and 1/2 (50%) common-variable immunodeficiency-associated DLBCL.]. 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:24496723; 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:NP1152104.RAz-Pil6DfAdYXkmH8xaY85Z9e4tWhYHi1mzKZ0z5cckQ130_publicationInfo { this: dcterms:created "2016-05-13T12:50:28+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }