@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:NP1022485.RAtHx2zt2dWU2sH20glDYafzTupcOaVLScjcXVYU305kQ130_head { this: np:hasAssertion dgn-np:NP1022485.RAtHx2zt2dWU2sH20glDYafzTupcOaVLScjcXVYU305kQ130_assertion; np:hasProvenance dgn-np:NP1022485.RAtHx2zt2dWU2sH20glDYafzTupcOaVLScjcXVYU305kQ130_provenance; np:hasPublicationInfo dgn-np:NP1022485.RAtHx2zt2dWU2sH20glDYafzTupcOaVLScjcXVYU305kQ130_publicationInfo; a np:Nanopublication . dgn-np:NP1022485.RAtHx2zt2dWU2sH20glDYafzTupcOaVLScjcXVYU305kQ130_assertion a np:Assertion . dgn-np:NP1022485.RAtHx2zt2dWU2sH20glDYafzTupcOaVLScjcXVYU305kQ130_provenance a np:Provenance . dgn-np:NP1022485.RAtHx2zt2dWU2sH20glDYafzTupcOaVLScjcXVYU305kQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP1022485.RAtHx2zt2dWU2sH20glDYafzTupcOaVLScjcXVYU305kQ130_assertion { miriam-gene:7535 a ncit:C16612 . lld:C0008626 a ncit:C7057 . dgn-gda:DGN1f9963f2a2579ebcf34e816953b07dbf sio:SIO_000628 miriam-gene:7535, lld:C0008626; a sio:SIO_001121 . } dgn-np:NP1022485.RAtHx2zt2dWU2sH20glDYafzTupcOaVLScjcXVYU305kQ130_provenance { dgn-np:NP1022485.RAtHx2zt2dWU2sH20glDYafzTupcOaVLScjcXVYU305kQ130_assertion dcterms:description "[We conclude that FISH for the detection of the most important chromosomal aberrations in CLL is an important laboratory parameter that is recommended for assessment and correlation with simultaneous evaluation of ZAP-70 and CD38 expression which could help in the prediction of outcome of CLL patients.]. 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:23082473; 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:NP1022485.RAtHx2zt2dWU2sH20glDYafzTupcOaVLScjcXVYU305kQ130_publicationInfo { this: dcterms:created "2016-05-13T12:49:29+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" . }