pubmed-article:20538168 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20538168 | lifeskim:mentions | umls-concept:C0035647 | lld:lifeskim |
pubmed-article:20538168 | lifeskim:mentions | umls-concept:C0003811 | lld:lifeskim |
pubmed-article:20538168 | lifeskim:mentions | umls-concept:C0023976 | lld:lifeskim |
pubmed-article:20538168 | lifeskim:mentions | umls-concept:C0429028 | lld:lifeskim |
pubmed-article:20538168 | lifeskim:mentions | umls-concept:C1826455 | lld:lifeskim |
pubmed-article:20538168 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
pubmed-article:20538168 | lifeskim:mentions | umls-concept:C2926735 | lld:lifeskim |
pubmed-article:20538168 | pubmed:issue | 24 | lld:pubmed |
pubmed-article:20538168 | pubmed:dateCreated | 2010-6-11 | lld:pubmed |
pubmed-article:20538168 | pubmed:abstractText | We investigated the role of nitric oxide 1 adaptor protein (NOS1AP) as a genetic modifier of long QT syndrome (LQTS). | lld:pubmed |
pubmed-article:20538168 | pubmed:language | eng | lld:pubmed |
pubmed-article:20538168 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20538168 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:20538168 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:20538168 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20538168 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20538168 | pubmed:month | Jun | lld:pubmed |
pubmed-article:20538168 | pubmed:issn | 1558-3597 | lld:pubmed |
pubmed-article:20538168 | pubmed:author | pubmed-author:ArkingDan EDE | lld:pubmed |
pubmed-article:20538168 | pubmed:author | pubmed-author:ChakravartiAr... | lld:pubmed |
pubmed-article:20538168 | pubmed:author | pubmed-author:BellazziRicca... | lld:pubmed |
pubmed-article:20538168 | pubmed:author | pubmed-author:PrioriSilvia... | lld:pubmed |
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pubmed-article:20538168 | pubmed:author | pubmed-author:BloiseRaffael... | lld:pubmed |
pubmed-article:20538168 | pubmed:author | pubmed-author:TomásMartaM | lld:pubmed |
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pubmed-article:20538168 | pubmed:author | pubmed-author:MaloviniAlber... | lld:pubmed |
pubmed-article:20538168 | pubmed:copyrightInfo | Copyright (c) 2010 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. | lld:pubmed |
pubmed-article:20538168 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20538168 | pubmed:day | 15 | lld:pubmed |
pubmed-article:20538168 | pubmed:volume | 55 | lld:pubmed |
pubmed-article:20538168 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20538168 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20538168 | pubmed:pagination | 2745-52 | lld:pubmed |
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pubmed-article:20538168 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20538168 | pubmed:articleTitle | Polymorphisms in the NOS1AP gene modulate QT interval duration and risk of arrhythmias in the long QT syndrome. | lld:pubmed |
pubmed-article:20538168 | pubmed:affiliation | Molecular Cardiology Laboratories, IRCCS Salvatore Maugeri Foundation, Pavia, Italy. | lld:pubmed |
pubmed-article:20538168 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20538168 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:20538168 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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