@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 Protein: . @prefix mgi: . @prefix geneProductOf: . @prefix RNA: . @prefix mesh: . @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 geneProductOf: mgi:1347477; a Protein: . sub:_2 geneProductOf: mgi:97501; a RNA: . sub:_3 occursIn: mesh:D008099, species:10090; rdf:object sub:_2; rdf:predicate belv:increases; rdf:subject sub:_1; a rdf:Statement . sub:assertion rdfs:label "p(MGI:Foxa3) -> r(MGI:Pck1)" . } 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 "1.4" . sub:_4 prov:value "A large number of liver-specific or liver-enriched genes which contain HNF3 binding sites have been described previously (reviewed in references 5, 7, 23, and 32). We wanted to know which of these genes are regulated by HNF3gamma in vivo. In order to address this question, we isolated total liver RNA from adult wild-type and mutant animals and analyzed the steady-state mRNA levels of various HNF3 targets by Northern blotting and RNase protection analysis. A subset of these results are shown in Fig. 5A, demonstrating that mRNA levels for TAT, Tf, and PEPCK are reduced in Hnf3g-/- mice, while those of G6Pase, serine dehydratase (SDH), TTR, and albumin are not changed."; prov:wasQuotedFrom pubmed:9632808 . sub:_5 rdfs:label "Selventa" . sub:assertion prov:hadPrimarySource pubmed:9632808; prov:wasDerivedFrom beldoc:, sub:_4 . } sub:pubinfo { this: dct:created "2014-07-03T14:31:00.007+02:00"^^xsd:dateTime; pav:createdBy orcid:0000-0001-6818-334X, orcid:0000-0002-1267-0234 . }