19350502

Source:http://linkedlifedata.com/resource/pubmed/id/19350502

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Subject	Predicate	Object	Context
pubmed-article:19350502	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:19350502	lifeskim:mentions	umls-concept:C0030705	lld:lifeskim
pubmed-article:19350502	lifeskim:mentions	umls-concept:C0015576	lld:lifeskim
pubmed-article:19350502	lifeskim:mentions	umls-concept:C0026847	lld:lifeskim
pubmed-article:19350502	lifeskim:mentions	umls-concept:C0017337	lld:lifeskim
pubmed-article:19350502	lifeskim:mentions	umls-concept:C1420295	lld:lifeskim
pubmed-article:19350502	lifeskim:mentions	umls-concept:C1416797	lld:lifeskim
pubmed-article:19350502	lifeskim:mentions	umls-concept:C0796357	lld:lifeskim
pubmed-article:19350502	pubmed:issue	2	lld:pubmed
pubmed-article:19350502	pubmed:dateCreated	2009-4-7	lld:pubmed
pubmed-article:19350502	pubmed:abstractText	To perform mutation analysis and describe the genotype of the SMN gene in a patient with spinal muscular atrophy (SMA) and his family.	lld:pubmed
pubmed-article:19350502	pubmed:language	chi	lld:pubmed
pubmed-article:19350502	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:19350502	pubmed:citationSubset	IM	lld:pubmed
pubmed-article:19350502	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:19350502	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:19350502	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:19350502	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:19350502	pubmed:month	Apr	lld:pubmed
pubmed-article:19350502	pubmed:issn	1003-9406	lld:pubmed
pubmed-article:19350502	pubmed:author	pubmed-author:CaiMei-yingMY	lld:pubmed
pubmed-article:19350502	pubmed:author	pubmed-author:ZengJianJ	lld:pubmed
pubmed-article:19350502	pubmed:author	pubmed-author:LanFeng-huaFH	lld:pubmed
pubmed-article:19350502	pubmed:author	pubmed-author:KeLong-fengLF	lld:pubmed
pubmed-article:19350502	pubmed:author	pubmed-author:YanAi-zhenAZ	lld:pubmed
pubmed-article:19350502	pubmed:author	pubmed-author:LinYan-hongYH	lld:pubmed
pubmed-article:19350502	pubmed:issnType	Print	lld:pubmed
pubmed-article:19350502	pubmed:volume	26	lld:pubmed
pubmed-article:19350502	pubmed:owner	NLM	lld:pubmed
pubmed-article:19350502	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:19350502	pubmed:pagination	139-43	lld:pubmed
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pubmed-article:19350502	pubmed:meshHeading	pubmed-meshheading:19350502...	lld:pubmed
pubmed-article:19350502	pubmed:meshHeading	pubmed-meshheading:19350502...	lld:pubmed
pubmed-article:19350502	pubmed:meshHeading	pubmed-meshheading:19350502...	lld:pubmed
pubmed-article:19350502	pubmed:meshHeading	pubmed-meshheading:19350502...	lld:pubmed
pubmed-article:19350502	pubmed:meshHeading	pubmed-meshheading:19350502...	lld:pubmed
pubmed-article:19350502	pubmed:meshHeading	pubmed-meshheading:19350502...	lld:pubmed
pubmed-article:19350502	pubmed:year	2009	lld:pubmed
pubmed-article:19350502	pubmed:articleTitle	[Mutation analysis of SMN gene in a patient and his family with spinal muscular atrophy].	lld:pubmed
pubmed-article:19350502	pubmed:affiliation	Fuzhou General Hospital, Nanjing Military Region, Fuzhou, Fujian, 350025 People's Republic of China.	lld:pubmed
pubmed-article:19350502	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:19350502	pubmed:publicationType	English Abstract	lld:pubmed
pubmed-article:19350502	pubmed:publicationType	Case Reports	lld:pubmed
pubmed-article:19350502	pubmed:publicationType	Research Support, Non-U.S. Gov't	lld:pubmed