pubmed-article:15928721 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:15928721 | lifeskim:mentions | umls-concept:C0014442 | lld:lifeskim |
pubmed-article:15928721 | lifeskim:mentions | umls-concept:C0949658 | lld:lifeskim |
pubmed-article:15928721 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
pubmed-article:15928721 | lifeskim:mentions | umls-concept:C0003011 | lld:lifeskim |
pubmed-article:15928721 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:15928721 | pubmed:dateCreated | 2005-6-1 | lld:pubmed |
pubmed-article:15928721 | pubmed:abstractText | Hypertrophic cardiomyopathy (HCM) is a genetic-based disease. Several gene mutations leading to HCM development have been described. | lld:pubmed |
pubmed-article:15928721 | pubmed:language | eng | lld:pubmed |
pubmed-article:15928721 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15928721 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:15928721 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15928721 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15928721 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15928721 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:15928721 | pubmed:month | May | lld:pubmed |
pubmed-article:15928721 | pubmed:issn | 0022-9032 | lld:pubmed |
pubmed-article:15928721 | pubmed:author | pubmed-author:MazurekUrszul... | lld:pubmed |
pubmed-article:15928721 | pubmed:author | pubmed-author:WilczokTadeus... | lld:pubmed |
pubmed-article:15928721 | pubmed:author | pubmed-author:WodnieckiJanJ | lld:pubmed |
pubmed-article:15928721 | pubmed:author | pubmed-author:Domal-Kwiatko... | lld:pubmed |
pubmed-article:15928721 | pubmed:author | pubmed-author:SmolikS?awomi... | lld:pubmed |
pubmed-article:15928721 | pubmed:author | pubmed-author:Nowalany-Kozi... | lld:pubmed |
pubmed-article:15928721 | pubmed:author | pubmed-author:WilczewskiPrz... | lld:pubmed |
pubmed-article:15928721 | pubmed:author | pubmed-author:GilanowskaGra... | lld:pubmed |
pubmed-article:15928721 | pubmed:author | pubmed-author:SzarekJaros?a... | lld:pubmed |
pubmed-article:15928721 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:15928721 | pubmed:volume | 62 | lld:pubmed |
pubmed-article:15928721 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:15928721 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:15928721 | pubmed:pagination | 440-9; 449-50 | lld:pubmed |
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pubmed-article:15928721 | pubmed:meshHeading | pubmed-meshheading:15928721... | lld:pubmed |
pubmed-article:15928721 | pubmed:year | 2005 | lld:pubmed |
pubmed-article:15928721 | pubmed:articleTitle | Familial hypertrophic cardiomyopathy. Insertion-deletion polymorphism of angiotensin-converting enzyme and angiotensin II receptor. | lld:pubmed |
pubmed-article:15928721 | pubmed:affiliation | 2nd chair and Department of Cardiology, Zabrze. | lld:pubmed |
pubmed-article:15928721 | pubmed:publicationType | Journal Article | lld:pubmed |