pubmed-article:17653048 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17653048 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:17653048 | lifeskim:mentions | umls-concept:C1556094 | lld:lifeskim |
pubmed-article:17653048 | lifeskim:mentions | umls-concept:C0035334 | lld:lifeskim |
pubmed-article:17653048 | lifeskim:mentions | umls-concept:C0035499 | lld:lifeskim |
pubmed-article:17653048 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:17653048 | lifeskim:mentions | umls-concept:C1708726 | lld:lifeskim |
pubmed-article:17653048 | lifeskim:mentions | umls-concept:C0220908 | lld:lifeskim |
pubmed-article:17653048 | lifeskim:mentions | umls-concept:C0018591 | lld:lifeskim |
pubmed-article:17653048 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
pubmed-article:17653048 | pubmed:dateCreated | 2007-7-26 | lld:pubmed |
pubmed-article:17653048 | pubmed:abstractText | To identify nucleotide sequence variations in the rhodopsin (RHO) gene of Japanese patients with retinitis pigmentosa (RP) in order to search for mutations or haplotypes responsible for RP. | lld:pubmed |
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pubmed-article:17653048 | pubmed:language | eng | lld:pubmed |
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pubmed-article:17653048 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:17653048 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17653048 | pubmed:issn | 1090-0535 | lld:pubmed |
pubmed-article:17653048 | pubmed:author | pubmed-author:KatoSeishiS | lld:pubmed |
pubmed-article:17653048 | pubmed:author | pubmed-author:OhmoriMasayuk... | lld:pubmed |
pubmed-article:17653048 | pubmed:author | pubmed-author:UsamiRonR | lld:pubmed |
pubmed-article:17653048 | pubmed:author | pubmed-author:YanashimaKenj... | lld:pubmed |
pubmed-article:17653048 | pubmed:author | pubmed-author:HataHiromiH | lld:pubmed |
pubmed-article:17653048 | pubmed:author | pubmed-author:OhtakeHidekiH | lld:pubmed |
pubmed-article:17653048 | pubmed:author | pubmed-author:ToyamaShigeru... | lld:pubmed |
pubmed-article:17653048 | pubmed:author | pubmed-author:OhtokoKuniyoK | lld:pubmed |
pubmed-article:17653048 | pubmed:author | pubmed-author:AndoYuichiroY | lld:pubmed |
pubmed-article:17653048 | pubmed:author | pubmed-author:O'hiraAyaA | lld:pubmed |
pubmed-article:17653048 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:17653048 | pubmed:volume | 13 | lld:pubmed |
pubmed-article:17653048 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17653048 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17653048 | pubmed:pagination | 1038-44 | lld:pubmed |
pubmed-article:17653048 | pubmed:dateRevised | 2010-9-15 | lld:pubmed |
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pubmed-article:17653048 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:17653048 | pubmed:articleTitle | Mutation screening and haplotype analysis of the rhodopsin gene locus in Japanese patients with retinitis pigmentosa. | lld:pubmed |
pubmed-article:17653048 | pubmed:affiliation | Department of Rehabilitation Engineering, Research Institute, National Rehabilitation Center for Persons with Disabilities, Tokorozawa, Saitama, Japan. | lld:pubmed |
pubmed-article:17653048 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17653048 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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