@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:NP1317903.RAWsv-ufRZ7inRI1U7TDALdGf6WfyQVFhERAgSme1HfTc130_head { this: np:hasAssertion dgn-np:NP1317903.RAWsv-ufRZ7inRI1U7TDALdGf6WfyQVFhERAgSme1HfTc130_assertion; np:hasProvenance dgn-np:NP1317903.RAWsv-ufRZ7inRI1U7TDALdGf6WfyQVFhERAgSme1HfTc130_provenance; np:hasPublicationInfo dgn-np:NP1317903.RAWsv-ufRZ7inRI1U7TDALdGf6WfyQVFhERAgSme1HfTc130_publicationInfo; a np:Nanopublication . dgn-np:NP1317903.RAWsv-ufRZ7inRI1U7TDALdGf6WfyQVFhERAgSme1HfTc130_assertion a np:Assertion . dgn-np:NP1317903.RAWsv-ufRZ7inRI1U7TDALdGf6WfyQVFhERAgSme1HfTc130_provenance a np:Provenance . dgn-np:NP1317903.RAWsv-ufRZ7inRI1U7TDALdGf6WfyQVFhERAgSme1HfTc130_publicationInfo a np:PublicationInfo . } dgn-np:NP1317903.RAWsv-ufRZ7inRI1U7TDALdGf6WfyQVFhERAgSme1HfTc130_assertion { miriam-gene:6545 a ncit:C16612 . lld:C0023434 a ncit:C7057 . dgn-gda:DGNa69c77ad6b5569583ac0657b13dccc38 sio:SIO_000628 miriam-gene:6545, lld:C0023434; a sio:SIO_001121 . } dgn-np:NP1317903.RAWsv-ufRZ7inRI1U7TDALdGf6WfyQVFhERAgSme1HfTc130_provenance { dgn-np:NP1317903.RAWsv-ufRZ7inRI1U7TDALdGf6WfyQVFhERAgSme1HfTc130_assertion dcterms:description "[However, a recent report indicated that VH251, one of three VH genes belonging to the VH5 subgroup (e.g., VH251, VH32, and VH15), not only is frequently rearranged in this disease, but also has extensive and selective mutations when expressed by CLL B cells.]. 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:7681468; 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:NP1317903.RAWsv-ufRZ7inRI1U7TDALdGf6WfyQVFhERAgSme1HfTc130_publicationInfo { this: dcterms:created "2016-05-13T12:51:43+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" . }