@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:NP127082.RATViaxOeedWFPTBj3GDFGE8lkdIzPOHkMTjmC8JHozTs130_head { this: np:hasAssertion dgn-np:NP127082.RATViaxOeedWFPTBj3GDFGE8lkdIzPOHkMTjmC8JHozTs130_assertion; np:hasProvenance dgn-np:NP127082.RATViaxOeedWFPTBj3GDFGE8lkdIzPOHkMTjmC8JHozTs130_provenance; np:hasPublicationInfo dgn-np:NP127082.RATViaxOeedWFPTBj3GDFGE8lkdIzPOHkMTjmC8JHozTs130_publicationInfo; a np:Nanopublication . dgn-np:NP127082.RATViaxOeedWFPTBj3GDFGE8lkdIzPOHkMTjmC8JHozTs130_assertion a np:Assertion . dgn-np:NP127082.RATViaxOeedWFPTBj3GDFGE8lkdIzPOHkMTjmC8JHozTs130_provenance a np:Provenance . dgn-np:NP127082.RATViaxOeedWFPTBj3GDFGE8lkdIzPOHkMTjmC8JHozTs130_publicationInfo a np:PublicationInfo . } dgn-np:NP127082.RATViaxOeedWFPTBj3GDFGE8lkdIzPOHkMTjmC8JHozTs130_assertion { miriam-gene:29888 a ncit:C16612 . lld:C0023434 a ncit:C7057 . dgn-gda:DGN26d8d12adea44cadb80ef5d1e0e10011 sio:SIO_000628 miriam-gene:29888, lld:C0023434; a sio:SIO_001122 . } dgn-np:NP127082.RATViaxOeedWFPTBj3GDFGE8lkdIzPOHkMTjmC8JHozTs130_provenance { dgn-np:NP127082.RATViaxOeedWFPTBj3GDFGE8lkdIzPOHkMTjmC8JHozTs130_assertion dcterms:description "[Our results confirm the previous findings and further support the role of a genetic basis in the etiology of CLL; however, more research is needed to elucidate the causal SNP(s) and the potential manner in which these SNPs or linked SNPs function in CLL p]. 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:20332261; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP127082.RATViaxOeedWFPTBj3GDFGE8lkdIzPOHkMTjmC8JHozTs130_publicationInfo { this: dcterms:created "2015-08-25T14:38:51+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }