18281613

Source:http://linkedlifedata.com/resource/pubmed/id/18281613

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Subject	Predicate	Object	Context
pubmed-article:18281613	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:18281613	lifeskim:mentions	umls-concept:C0035309	lld:lifeskim
pubmed-article:18281613	lifeskim:mentions	umls-concept:C0271097	lld:lifeskim
pubmed-article:18281613	lifeskim:mentions	umls-concept:C0017337	lld:lifeskim
pubmed-article:18281613	lifeskim:mentions	umls-concept:C0026882	lld:lifeskim
pubmed-article:18281613	lifeskim:mentions	umls-concept:C1314792	lld:lifeskim
pubmed-article:18281613	pubmed:issue	6	lld:pubmed
pubmed-article:18281613	pubmed:dateCreated	2008-6-2	lld:pubmed
pubmed-article:18281613	pubmed:abstractText	To determine the retinal phenotype of Usher syndrome type III (USH3A) caused by clarin-1 (CLRN1) gene mutations in a non-Finnish population.	lld:pubmed
pubmed-article:18281613	pubmed:language	eng	lld:pubmed
pubmed-article:18281613	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:18281613	pubmed:citationSubset	IM	lld:pubmed
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pubmed-article:18281613	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:18281613	pubmed:month	Jun	lld:pubmed
pubmed-article:18281613	pubmed:issn	0146-0404	lld:pubmed
pubmed-article:18281613	pubmed:author	pubmed-author:JacobsonSamue...	lld:pubmed
pubmed-article:18281613	pubmed:author	pubmed-author:CideciyanArtu...	lld:pubmed
pubmed-article:18281613	pubmed:author	pubmed-author:AlemanTomas...	lld:pubmed
pubmed-article:18281613	pubmed:author	pubmed-author:StoneEdwin...	lld:pubmed
pubmed-article:18281613	pubmed:author	pubmed-author:KimberlingWil...	lld:pubmed
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pubmed-article:18281613	pubmed:author	pubmed-author:SchwartzSharo...	lld:pubmed
pubmed-article:18281613	pubmed:author	pubmed-author:Ben-YosefTama...	lld:pubmed
pubmed-article:18281613	pubmed:author	pubmed-author:LiuXue-ZhongX...	lld:pubmed
pubmed-article:18281613	pubmed:author	pubmed-author:WindsorElizab...	lld:pubmed
pubmed-article:18281613	pubmed:author	pubmed-author:RomanAlejandr...	lld:pubmed
pubmed-article:18281613	pubmed:author	pubmed-author:HerreraWaldoW	lld:pubmed
pubmed-article:18281613	pubmed:issnType	Print	lld:pubmed
pubmed-article:18281613	pubmed:volume	49	lld:pubmed
pubmed-article:18281613	pubmed:owner	NLM	lld:pubmed
pubmed-article:18281613	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:18281613	pubmed:pagination	2651-60	lld:pubmed
pubmed-article:18281613	pubmed:dateRevised	2010-11-18	lld:pubmed
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pubmed-article:18281613	pubmed:meshHeading	pubmed-meshheading:18281613...	lld:pubmed
pubmed-article:18281613	pubmed:year	2008	lld:pubmed
pubmed-article:18281613	pubmed:articleTitle	Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene.	lld:pubmed
pubmed-article:18281613	pubmed:affiliation	Scheie Eye Institute, Department of Ophthalmology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.	lld:pubmed
pubmed-article:18281613	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:18281613	pubmed:publicationType	Research Support, Non-U.S. Gov't	lld:pubmed
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