@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 hgnc: . @prefix geneProductOf: . @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 geneProductOf: hgnc:5472; a RNA: . sub:_2 occursIn: species:9606; rdf:object sub:_1; rdf:predicate belv:decreases; rdf:subject chebi:50113; a rdf:Statement . sub:assertion rdfs:label "a(CHEBI:androgen) -| r(HGNC:IGFBP3)" . } 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 "On treatment of LNCaP cells with R1881 (a synthetic androgen) it was observed that IGFBP-3 was markedly suppressed both by high and low concentrations of R1881. Levels of IGFBP-3 tended to be lower in biopsies from cancer patients as compared to patients with benign prostatic hyperplasia. It was further found that the marked increase in IGFBP-3 induced by ATRA was largely neutralized by androgen."; prov:wasQuotedFrom pubmed:10580834 . sub:_4 rdfs:label "Selventa" . sub:assertion prov:hadPrimarySource pubmed:10580834; prov:wasDerivedFrom beldoc:, sub:_3 . } sub:pubinfo { this: dct:created "2014-07-03T14:29:49.388+02:00"^^xsd:dateTime; pav:createdBy orcid:0000-0001-6818-334X, orcid:0000-0002-1267-0234 . }