@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:NP1288185.RAdBly86A-23VJQ0hOz0rZk3pFQ0tRf4yEt9ANm66e_JI130_head { this: np:hasAssertion dgn-np:NP1288185.RAdBly86A-23VJQ0hOz0rZk3pFQ0tRf4yEt9ANm66e_JI130_assertion; np:hasProvenance dgn-np:NP1288185.RAdBly86A-23VJQ0hOz0rZk3pFQ0tRf4yEt9ANm66e_JI130_provenance; np:hasPublicationInfo dgn-np:NP1288185.RAdBly86A-23VJQ0hOz0rZk3pFQ0tRf4yEt9ANm66e_JI130_publicationInfo; a np:Nanopublication . dgn-np:NP1288185.RAdBly86A-23VJQ0hOz0rZk3pFQ0tRf4yEt9ANm66e_JI130_assertion a np:Assertion . dgn-np:NP1288185.RAdBly86A-23VJQ0hOz0rZk3pFQ0tRf4yEt9ANm66e_JI130_provenance a np:Provenance . dgn-np:NP1288185.RAdBly86A-23VJQ0hOz0rZk3pFQ0tRf4yEt9ANm66e_JI130_publicationInfo a np:PublicationInfo . } dgn-np:NP1288185.RAdBly86A-23VJQ0hOz0rZk3pFQ0tRf4yEt9ANm66e_JI130_assertion { miriam-gene:330 a ncit:C16612 . lld:C0596263 a ncit:C7057 . dgn-gda:DGNabbd734d5b0084e6d338cbf23eb782c1 sio:SIO_000628 miriam-gene:330, lld:C0596263; a sio:SIO_001121 . } dgn-np:NP1288185.RAdBly86A-23VJQ0hOz0rZk3pFQ0tRf4yEt9ANm66e_JI130_provenance { dgn-np:NP1288185.RAdBly86A-23VJQ0hOz0rZk3pFQ0tRf4yEt9ANm66e_JI130_assertion dcterms:description "[Copy number loss for and somatic mutation of BIRC2 and BIRC3 have been frequently detected in lymphoid malignancies, with such genetic alterations being thought to contribute to carcinogenesis through activation of the noncanonical NF-κB signaling pathway.]. 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:26094954; 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:NP1288185.RAdBly86A-23VJQ0hOz0rZk3pFQ0tRf4yEt9ANm66e_JI130_publicationInfo { this: dcterms:created "2016-05-13T12:51:30+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" . }