@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 go: . @prefix RNA: . @prefix hgnc: . @prefix geneProductOf: . @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 geneProductOf: hgnc:20844; a RNA: . sub:_2 occursIn: obo:CL_0000115, obo:UBERON_0000947, species:9606; rdf:object sub:_1; rdf:predicate belv:decreases; rdf:subject go:0001666; a rdf:Statement . sub:assertion rdfs:label "bp(GOBP:\"response to hypoxia\") -| r(HGNC:GPR156)" . } 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 "20131211" . sub:_3 prov:value "Gene expression changes in other functional groups. Hypoxia also resulted in an increase in the expression of vascular endothelial growth factor C (VEGFC), although this was not statistically significant. Additionally, we observed a significant increase in the expression of plasminogen activator inhibitor type 1 (SERPINE1). This increase was confirmed by real-time RT-PCR (Fig. 1). We also found that a number of genes encoding proteins involved in mediating a cytoprotective response to oxidant stress were reduced by hypoxia, including metallothionein 2A (MT2A), biliverdin reductase A (BLVRA), and GABAB-related G-protein coupled receptor (GABABL)."; prov:wasQuotedFrom pubmed:15100389 . sub:_4 rdfs:label "Selventa" . sub:assertion prov:hadPrimarySource pubmed:15100389; prov:wasDerivedFrom beldoc:, sub:_3 . } sub:pubinfo { this: dct:created "2014-07-03T14:32:20.182+02:00"^^xsd:dateTime; pav:createdBy orcid:0000-0001-6818-334X, orcid:0000-0002-1267-0234 . }