@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 Protein: . @prefix hgnc: . @prefix geneProductOf: . @prefix hasAgent: . @prefix RNA: . @prefix species: . @prefix occursIn: . @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:13875; a Protein: . sub:_3 geneProductOf: hgnc:16709; a RNA: . sub:_4 occursIn: species:9606; rdf:object sub:_3; rdf:predicate belv:directlyDecreases; rdf:subject sub:_1; a rdf:Statement . sub:assertion rdfs:label "tscript(p(HGNC:FOXP2)) =| r(HGNC:CALCRL)" . } 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:_6; pav:version "1.4" . sub:_5 prov:value "In line with previous studies suggesting that FOXP proteins act as repressors,14,18,38 10 of the targets tested (SLC17A3, CALCRL, LNPEP, HSPB7, CER1, COX11, PM5, PSEN2, CD164, and RCN2) showed reduced expression in the presence of FOXP2. However, two genes (MAPK8IP and SYK) displayed significant increases in transcription in response to FOXP2 upregulation in our stable cell lines. EMSAs and ChIP also performed indicating direct promoter binding."; prov:wasQuotedFrom pubmed:17999362 . sub:_6 rdfs:label "Selventa" . sub:assertion prov:hadPrimarySource pubmed:17999362; prov:wasDerivedFrom beldoc:, sub:_5 . } sub:pubinfo { this: dct:created "2014-07-03T14:30:52.246+02:00"^^xsd:dateTime; pav:createdBy orcid:0000-0001-6818-334X, orcid:0000-0002-1267-0234 . }