@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:NP397051.RAm2G3CH2UMux_yerLrboguDXg6u7ttgVPTBuGHRluq_I130_head { this: np:hasAssertion dgn-np:NP397051.RAm2G3CH2UMux_yerLrboguDXg6u7ttgVPTBuGHRluq_I130_assertion; np:hasProvenance dgn-np:NP397051.RAm2G3CH2UMux_yerLrboguDXg6u7ttgVPTBuGHRluq_I130_provenance; np:hasPublicationInfo dgn-np:NP397051.RAm2G3CH2UMux_yerLrboguDXg6u7ttgVPTBuGHRluq_I130_publicationInfo; a np:Nanopublication . dgn-np:NP397051.RAm2G3CH2UMux_yerLrboguDXg6u7ttgVPTBuGHRluq_I130_assertion a np:Assertion . dgn-np:NP397051.RAm2G3CH2UMux_yerLrboguDXg6u7ttgVPTBuGHRluq_I130_provenance a np:Provenance . dgn-np:NP397051.RAm2G3CH2UMux_yerLrboguDXg6u7ttgVPTBuGHRluq_I130_publicationInfo a np:PublicationInfo . } dgn-np:NP397051.RAm2G3CH2UMux_yerLrboguDXg6u7ttgVPTBuGHRluq_I130_assertion { miriam-gene:2214 a ncit:C16612 . lld:C0014522 a ncit:C7057 . dgn-gda:DGN7b3cd5fb4b6f724fb6539300942bbdd8 sio:SIO_000628 miriam-gene:2214, lld:C0014522; a sio:SIO_001123 . } dgn-np:NP397051.RAm2G3CH2UMux_yerLrboguDXg6u7ttgVPTBuGHRluq_I130_provenance { dgn-np:NP397051.RAm2G3CH2UMux_yerLrboguDXg6u7ttgVPTBuGHRluq_I130_assertion dcterms:description "[However, supershift assays using the available mAb recognizing the T cell NFATc revealed no detectable NFATc protein in nuclear and cytoplasmic extracts from CD16- or phorbol ester-stimulated cells at any time tested, up to 4 h. These results provide the first direct evidence that both CsA-sensitive transcription factors, NFATp and NFATc, are expressed in human NK cells, and that their activation and/or expression can be regulated in primary cells by a single stimulus, that, in the case of CD16 in NK cells, results in early activation of NFATp and subsequently induced expression of NFATc mRNA.]. 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:7650486; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP397051.RAm2G3CH2UMux_yerLrboguDXg6u7ttgVPTBuGHRluq_I130_publicationInfo { this: dcterms:created "2015-08-25T14:41:31+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" . }