@prefix dc: . @prefix this: . @prefix sub: . @prefix beldoc: . @prefix rdfs: . @prefix rdf: . @prefix xsd: . @prefix dce: . @prefix pav: . @prefix np: . @prefix belv: . @prefix prov: . @prefix hgnc: . @prefix proteinModification: . @prefix mesh: . @prefix occursIn: . @prefix hasAnnotation: . @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 belv:hasSubstitution "M,229,L"; belv:variantOf hgnc:12517; a proteinModification: . sub:_2 occursIn: mesh:D052437, species:9606; hasAnnotation: sub:_3; rdf:object mesh:D003924; rdf:predicate belv:positiveCorrelation; rdf:subject sub:_1; a rdf:Statement . sub:_3 dc:subject "TextLocation"; rdf:value "Review" . sub:assertion rdfs:label "p(HGNC:UCP1,sub(M,229,L)) positiveCorrelation path(MESHD:\"Diabetes Mellitus, Type 2\")" . } sub:provenance { beldoc: dce:description "Approximately 2000 hand curated statements drawn from 57 PubMeds."; dce:rights "Copyright (c) 2011-2012, Selventa. All Rights Reserved."; dce:title "BEL Framework Small Corpus Document"; dc:license "Creative Commons Attribution-Non-Commercial-ShareAlike 3.0 Unported License"; pav:authoredBy sub:_5; pav:version "1.6" . sub:_4 prov:value """They found an A/C transition in the 5' untranslated region of exon 1 (112 bp upstream of the translation initiation codon) and also a Met229/Leu variant. Interestingly, the allele frequencies for the C variant and for the Leu229 variant were higher in the Type 2 diabetic group than in the control group."""; prov:wasQuotedFrom pubmed:15777261 . sub:_5 rdfs:comment "support@belframework.org"; rdfs:label "Selventa" . sub:assertion prov:hadPrimarySource pubmed:15777261; prov:wasDerivedFrom beldoc:, sub:_4 . } sub:pubinfo { this: dc:created "2014-07-03T14:29:32.456+02:00"^^xsd:dateTime; pav:createdBy orcid:0000-0001-6818-334X, orcid:0000-0002-1267-0234 . }