@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 RNA: . @prefix mgi: . @prefix geneProductOf: . @prefix species: . @prefix occursIn: . @prefix mesh: . @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 geneProductOf: mgi:96820; a RNA: . sub:_2 occursIn: mesh:D008264, species:10090; rdf:object sub:_1; rdf:predicate belv:increases; rdf:subject chebi:44952; a rdf:Statement . sub:assertion rdfs:label "a(CHEBI:\"palmitic acid\") -> r(MGI:Lpl)" . } 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:_4; pav:version "1.4" . sub:_3 prov:value "Incubation...with LA, PA, and SA significantly increased Mo LPL mRNA expression. expose of macrophages to AA and EPA dramatically decreased LPL mRNA levels... These results suggest that FAs, including PA, SA, and AA, might exert their regulatory effect on Mo LPL gene expression, at least partly, through a PPAR-dependent mechanism. Indeed, we found that these well-characterized ligands and activators of PPARs (49) directly regulate Mo LPL gene expression and enhance the binding activity of nuclear proteins to the PPRE element present in the LPL gene in a PPAR-specific manner."; prov:wasQuotedFrom pubmed:11246888 . sub:_4 rdfs:label "Selventa" . sub:assertion prov:hadPrimarySource pubmed:11246888; prov:wasDerivedFrom beldoc:, sub:_3 . } sub:pubinfo { this: dct:created "2014-07-03T14:29:54.616+02:00"^^xsd:dateTime; pav:createdBy orcid:0000-0001-6818-334X, orcid:0000-0002-1267-0234 . }