@prefix this: . @prefix sub: . @prefix beldoc: . @prefix rdfs: . @prefix rdf: . @prefix xsd: . @prefix dct: . @prefix dce: . @prefix pav: . @prefix np: . @prefix belv: . @prefix prov: . @prefix chebi: . @prefix go: . @prefix Protein: . @prefix hgnc: . @prefix geneProductOf: . @prefix hasAgent: . @prefix obo: . @prefix occursIn: . @prefix species: . @prefix pubmed: . @prefix orcid: . sub:Head { this: np:hasAssertion sub:assertion; np:hasProvenance sub:provenance; np:hasPublicationInfo sub:pubinfo; a np:Nanopublication . } sub:assertion { sub:_1 hasAgent: sub:_2; a go:0042789 . sub:_2 geneProductOf: hgnc:7782; a Protein: . sub:_3 occursIn: obo:CLO_0001925, species:9606; rdf:object sub:_1; rdf:predicate belv:increases; rdf:subject chebi:5586; a rdf:Statement . sub:assertion rdfs:label "a(CHEBI:\"hydrogen peroxide\") -> tscript(p(HGNC:NFE2L2))" . } sub:provenance { beldoc: dce:description "Approximately 61,000 statements."; dce:rights "Copyright (c) 2011-2012, Selventa. All rights reserved."; dce:title "BEL Framework Large Corpus Document"; pav:authoredBy sub:_5; pav:version "20131211" . sub:_4 prov:value "BEAS2B cells were retransfected with the NQO1– ARE reporter vector. Twenty-four hours after the second transfection, cells were treated with H2O2 (200 ?M), 2,5-tert-butylhydroquinone (TBHQ) (50 ?M), and CS extract (100 ?g/ml) for 12 h and luciferase activity was measured. As shown in Fig. 2C, BEAS2B cells transfected with NS siRNA displayed a significant increase in the amount of ARE luciferase activity in response to treatment with oxidative stressinducing agents, whereas Nrf2 siRNA-transfected cells showed significantly reduced NQO1–ARE–luciferase induction."; prov:wasQuotedFrom pubmed:19027064 . sub:_5 rdfs:label "Selventa" . sub:assertion prov:hadPrimarySource pubmed:19027064; prov:wasDerivedFrom beldoc:, sub:_4 . } sub:pubinfo { this: dct:created "2014-07-03T14:33:29.391+02:00"^^xsd:dateTime; pav:createdBy orcid:0000-0001-6818-334X, orcid:0000-0002-1267-0234 . }