18841006

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Subject	Predicate	Object	Context
pubmed-article:18841006	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:18841006	lifeskim:mentions	umls-concept:C0030705	lld:lifeskim
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pubmed-article:18841006	lifeskim:mentions	umls-concept:C0007785	lld:lifeskim
pubmed-article:18841006	lifeskim:mentions	umls-concept:C0026882	lld:lifeskim
pubmed-article:18841006	lifeskim:mentions	umls-concept:C1412058	lld:lifeskim
pubmed-article:18841006	lifeskim:mentions	umls-concept:C0205396	lld:lifeskim
pubmed-article:18841006	lifeskim:mentions	umls-concept:C0679622	lld:lifeskim
pubmed-article:18841006	lifeskim:mentions	umls-concept:C0205314	lld:lifeskim
pubmed-article:18841006	pubmed:issue	3	lld:pubmed
pubmed-article:18841006	pubmed:dateCreated	2008-10-20	lld:pubmed
pubmed-article:18841006	pubmed:abstractText	To date, 81 mutations of ATP-binding cassette transporter 1 (ABCA1) have been reported. However, no ABCA1 mutation has been reported in the Chinese population.	lld:pubmed
pubmed-article:18841006	pubmed:language	eng	lld:pubmed
pubmed-article:18841006	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:18841006	pubmed:citationSubset	IM	lld:pubmed
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pubmed-article:18841006	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:18841006	pubmed:issn	1421-9824	lld:pubmed
pubmed-article:18841006	pubmed:author	pubmed-author:ItôHH	lld:pubmed
pubmed-article:18841006	pubmed:author	pubmed-author:WangNingN	lld:pubmed
pubmed-article:18841006	pubmed:author	pubmed-author:WuZhi-YingZY	lld:pubmed
pubmed-article:18841006	pubmed:author	pubmed-author:FangLingL	lld:pubmed
pubmed-article:18841006	pubmed:author	pubmed-author:ZhaoGui-XianG...	lld:pubmed
pubmed-article:18841006	pubmed:author	pubmed-author:XueXie-HuaXH	lld:pubmed
pubmed-article:18841006	pubmed:author	pubmed-author:MurongShenxin...	lld:pubmed
pubmed-article:18841006	pubmed:copyrightInfo	Copyright 2008 S. Karger AG, Basel.	lld:pubmed
pubmed-article:18841006	pubmed:issnType	Electronic	lld:pubmed
pubmed-article:18841006	pubmed:volume	26	lld:pubmed
pubmed-article:18841006	pubmed:owner	NLM	lld:pubmed
pubmed-article:18841006	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:18841006	pubmed:pagination	234-8	lld:pubmed
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pubmed-article:18841006	pubmed:meshHeading	pubmed-meshheading:18841006...	lld:pubmed
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pubmed-article:18841006	pubmed:meshHeading	pubmed-meshheading:18841006...	lld:pubmed
pubmed-article:18841006	pubmed:year	2008	lld:pubmed
pubmed-article:18841006	pubmed:articleTitle	Novel mutation in the ABCA1 gene identified in a chinese patient with dementia and atherothrombotic cerebral infarction.	lld:pubmed
pubmed-article:18841006	pubmed:affiliation	Department of Neurology and Institute of Neurology, First Affiliated Hospital, Center of Neuroscience, Fujian Medical University, Fuzhou, China.	lld:pubmed
pubmed-article:18841006	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:18841006	pubmed:publicationType	Case Reports	lld:pubmed
pubmed-article:18841006	pubmed:publicationType	Research Support, Non-U.S. Gov't	lld:pubmed
entrez-gene:19	entrezgene:pubmed	pubmed-article:18841006	lld:entrezgene
http://linkedlifedata.com/r...	entrezgene:pubmed	pubmed-article:18841006	lld:entrezgene
http://linkedlifedata.com/r...	entrezgene:pubmed	pubmed-article:18841006	lld:entrezgene
lhgdn:association:55033	lhgdn:found_in	pubmed-article:18841006	lld:lhgdn