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2012年论文 наукова стаття, опублікована в травні 2012 2012年の論文 artigo científico (publicado na 2012) vetenskaplig artikel wissenschaftlicher Artikel tieteellinen artikkeli مقالهٔ علمی 2012年論文 บทความทางวิทยาศาสตร์ artigo científico videnskabelig artikel (udgivet 2012) գիտական հոդված vědecký článek vitenskapelig artikkel 2012年论文 2012 nî lūn-bûn article científic مقالة علمية научная статья vitskapeleg artikkel სამეცნიერო სტატია 2012年论文 2012年論文 artikull shkencor artigo científico (publicado na 2012) سائنسی مضمون articolo scientifico научни чланак vedecký článok bài báo khoa học mokslinis straipsnis artículu científicu espublizáu en 2012 2012年论文 2012年論文 wetenschappelijk artikel ২০১২-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ scientific article article scientific bilimsel makale scienca artikolo 2012년 논문 2012年論文 teaduslik artikkel artículo científico publicado en 2012 naučni članak мақолаи илмӣ articol științific מאמר מדעי επιστημονικό άρθρο мақолаи илмӣ 2012年论文 artykuł naukowy artikulong pang-agham article scientifique (publié 2012) tudományos cikk научни чланак научна статия 2012年论文 2012年論文
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2012-05-03T00:00:00Z
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wdt:P2093
Satish Kumar John Powell Carl W Cotman Jason JiYong Lee Jessica R Lane Eric Klein Richard J Caselli Subashchandrabose Chinnathambi Salvatore Spina Andrew Kertesz Jacek Biernat Thomas D Bird Wallace W Tourtellotte Li-San Wang Chris Zarow Virginia M Lee
rdfs:label
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
skos:prefLabel
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
schema:name
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
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