PMC:4195273 / 81715-82122 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/4195273","sourcedb":"PMC","sourceid":"4195273","source_url":"https://www.ncbi.nlm.nih.gov/pmc/4195273","text":"Guerardel et al., 2005 Sequence variability screen and haplotype analysis French Caucasian (989) Morbidly obese (621) and non-obese controls (368) 5′ SNPs: −3608T\u003eC, −3607C\u003eT, −1702C\u003eT, −175A\u003eG; 3′UTR SNP: ΔA1457 Higher allele frequencies in morbidly obese subjects than controls; association enhanced with the SNP haplotype structure 3608T\u003eC (or 175A\u003eG) and −1702C\u003eT, combined to ΔA1457 N/A N/A N/A","divisions":[{"label":"td","span":{"begin":0,"end":22}},{"label":"td","span":{"begin":24,"end":74}},{"label":"td","span":{"begin":76,"end":98}},{"label":"td","span":{"begin":100,"end":149}},{"label":"td","span":{"begin":151,"end":216}},{"label":"td","span":{"begin":218,"end":392}},{"label":"td","span":{"begin":394,"end":397}},{"label":"td","span":{"begin":399,"end":402}}],"tracks":[{"project":"TEST0","denotations":[{"id":"25352770-235-243-357878","span":{"begin":18,"end":22},"obj":"[\"15823203\"]"}],"attributes":[{"subj":"25352770-235-243-357878","pred":"source","obj":"TEST0"}]},{"project":"0_colil","denotations":[{"id":"25352770-15823203-357878","span":{"begin":18,"end":22},"obj":"15823203"}],"attributes":[{"subj":"25352770-15823203-357878","pred":"source","obj":"0_colil"}]},{"project":"2_test","denotations":[{"id":"25352770-15823203-38284867","span":{"begin":18,"end":22},"obj":"15823203"}],"attributes":[{"subj":"25352770-15823203-38284867","pred":"source","obj":"2_test"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"TEST0","color":"#e6ec93","default":true},{"id":"0_colil","color":"#d793ec"},{"id":"2_test","color":"#93ecbd"}]}]}}