@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 .
}