pubmed-article:20431721 | rdf:type | pubmed:Citation | lld:pubmed |
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pubmed-article:20431721 | lifeskim:mentions | umls-concept:C0152035 | lld:lifeskim |
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pubmed-article:20431721 | lifeskim:mentions | umls-concept:C0599155 | lld:lifeskim |
pubmed-article:20431721 | lifeskim:mentions | umls-concept:C0110614 | lld:lifeskim |
pubmed-article:20431721 | lifeskim:mentions | umls-concept:C1415071 | lld:lifeskim |
pubmed-article:20431721 | lifeskim:mentions | umls-concept:C0205396 | lld:lifeskim |
pubmed-article:20431721 | lifeskim:mentions | umls-concept:C0796357 | lld:lifeskim |
pubmed-article:20431721 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
pubmed-article:20431721 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
pubmed-article:20431721 | pubmed:dateCreated | 2010-4-30 | lld:pubmed |
pubmed-article:20431721 | pubmed:abstractText | To identify the genetic defects in a three-generation Chinese family with congenital nuclear cataract. | lld:pubmed |
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pubmed-article:20431721 | pubmed:language | eng | lld:pubmed |
pubmed-article:20431721 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20431721 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:20431721 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20431721 | pubmed:issn | 1090-0535 | lld:pubmed |
pubmed-article:20431721 | pubmed:author | pubmed-author:XXX | lld:pubmed |
pubmed-article:20431721 | pubmed:author | pubmed-author:HSUJ YJY | lld:pubmed |
pubmed-article:20431721 | pubmed:author | pubmed-author:ZhouNanN | lld:pubmed |
pubmed-article:20431721 | pubmed:author | pubmed-author:QiYanhuaY | lld:pubmed |
pubmed-article:20431721 | pubmed:author | pubmed-author:WangBinbinB | lld:pubmed |
pubmed-article:20431721 | pubmed:author | pubmed-author:ZhouShiyiS | lld:pubmed |
pubmed-article:20431721 | pubmed:author | pubmed-author:HuShanshanS | lld:pubmed |
pubmed-article:20431721 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20431721 | pubmed:volume | 16 | lld:pubmed |
pubmed-article:20431721 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20431721 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20431721 | pubmed:pagination | 713-9 | lld:pubmed |
pubmed-article:20431721 | pubmed:dateRevised | 2010-9-30 | lld:pubmed |
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pubmed-article:20431721 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20431721 | pubmed:articleTitle | Mutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3). | lld:pubmed |
pubmed-article:20431721 | pubmed:affiliation | Department of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China. | lld:pubmed |
pubmed-article:20431721 | pubmed:publicationType | Journal Article | lld:pubmed |