21174522

Source:http://linkedlifedata.com/resource/pubmed/id/21174522

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Subject	Predicate	Object	Context
pubmed-article:21174522	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:21174522	lifeskim:mentions	umls-concept:C0015576	lld:lifeskim
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pubmed-article:21174522	lifeskim:mentions	umls-concept:C0439660	lld:lifeskim
pubmed-article:21174522	lifeskim:mentions	umls-concept:C0392557	lld:lifeskim
pubmed-article:21174522	lifeskim:mentions	umls-concept:C1415075	lld:lifeskim
pubmed-article:21174522	lifeskim:mentions	umls-concept:C0796345	lld:lifeskim
pubmed-article:21174522	lifeskim:mentions	umls-concept:C1513778	lld:lifeskim
pubmed-article:21174522	pubmed:issue	1	lld:pubmed
pubmed-article:21174522	pubmed:dateCreated	2011-2-23	lld:pubmed
pubmed-article:21174522	pubmed:abstractText	The aim of the study was to characterize the underlying mutation in a large multiplex Chinese family with hereditary nuclear cataract.	lld:pubmed
pubmed-article:21174522	pubmed:language	eng	lld:pubmed
pubmed-article:21174522	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
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pubmed-article:21174522	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:21174522	pubmed:month	Mar	lld:pubmed
pubmed-article:21174522	pubmed:issn	1744-5094	lld:pubmed
pubmed-article:21174522	pubmed:author	pubmed-author:XuZ CZC	lld:pubmed
pubmed-article:21174522	pubmed:author	pubmed-author:ZhuX NXN	lld:pubmed
pubmed-article:21174522	pubmed:author	pubmed-author:BiY HYH	lld:pubmed
pubmed-article:21174522	pubmed:author	pubmed-author:SeulBB	lld:pubmed
pubmed-article:21174522	pubmed:author	pubmed-author:ZhangFengF	lld:pubmed
pubmed-article:21174522	pubmed:author	pubmed-author:Mse	lld:pubmed
pubmed-article:21174522	pubmed:author	pubmed-author:WangDuen-MeiD...	lld:pubmed
pubmed-article:21174522	pubmed:author	pubmed-author:HuSongnianS	lld:pubmed
pubmed-article:21174522	pubmed:author	pubmed-author:LingXuX	lld:pubmed
pubmed-article:21174522	pubmed:author	pubmed-author:ChenJiajingJ	lld:pubmed
pubmed-article:21174522	pubmed:author	pubmed-author:DaiQiushiQ	lld:pubmed
pubmed-article:21174522	pubmed:issnType	Electronic	lld:pubmed
pubmed-article:21174522	pubmed:volume	32	lld:pubmed
pubmed-article:21174522	pubmed:owner	NLM	lld:pubmed
pubmed-article:21174522	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:21174522	pubmed:pagination	48-53	lld:pubmed
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pubmed-article:21174522	pubmed:year	2011	lld:pubmed
pubmed-article:21174522	pubmed:articleTitle	Genetic linkage analyses and Cx50 mutation detection in a large multiplex Chinese family with hereditary nuclear cataract.	lld:pubmed
pubmed-article:21174522	pubmed:affiliation	Shenyang He Eye Hospital, He College of Ophthalmology and Visual Science, Shenyang, China.	lld:pubmed
pubmed-article:21174522	pubmed:publicationType	Journal Article	lld:pubmed
entrez-gene:2703	entrezgene:pubmed	pubmed-article:21174522	lld:entrezgene
http://linkedlifedata.com/r...	entrezgene:pubmed	pubmed-article:21174522	lld:entrezgene