| pubmed-article:8240107 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8240107 | lifeskim:mentions | umls-concept:C0012634 | lld:lifeskim |
| pubmed-article:8240107 | lifeskim:mentions | umls-concept:C0035334 | lld:lifeskim |
| pubmed-article:8240107 | lifeskim:mentions | umls-concept:C0035499 | lld:lifeskim |
| pubmed-article:8240107 | lifeskim:mentions | umls-concept:C0009221 | lld:lifeskim |
| pubmed-article:8240107 | lifeskim:mentions | umls-concept:C0443147 | lld:lifeskim |
| pubmed-article:8240107 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:8240107 | lifeskim:mentions | umls-concept:C0596611 | lld:lifeskim |
| pubmed-article:8240107 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:8240107 | pubmed:dateCreated | 1993-12-7 | lld:pubmed |
| pubmed-article:8240107 | pubmed:abstractText | To ascertain and characterize rhodopsin gene mutations in autosomal dominant retinitis pigmentosa and to correlate these mutations with the clinical phenotypes. | lld:pubmed |
| pubmed-article:8240107 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8240107 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8240107 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:8240107 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8240107 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:8240107 | pubmed:issn | 0003-9950 | lld:pubmed |
| pubmed-article:8240107 | pubmed:author | pubmed-author:CottonR GRG | lld:pubmed |
| pubmed-article:8240107 | pubmed:author | pubmed-author:SullivanL JLJ | lld:pubmed |
| pubmed-article:8240107 | pubmed:author | pubmed-author:ForrestSS | lld:pubmed |
| pubmed-article:8240107 | pubmed:author | pubmed-author:LoughnanM SMS | lld:pubmed |
| pubmed-article:8240107 | pubmed:author | pubmed-author:DickinsonPP | lld:pubmed |
| pubmed-article:8240107 | pubmed:author | pubmed-author:MakrisG SGS | lld:pubmed |
| pubmed-article:8240107 | pubmed:author | pubmed-author:MulhallL ELE | lld:pubmed |
| pubmed-article:8240107 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8240107 | pubmed:volume | 111 | lld:pubmed |
| pubmed-article:8240107 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8240107 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8240107 | pubmed:pagination | 1512-7 | lld:pubmed |
| pubmed-article:8240107 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:8240107 | pubmed:year | 1993 | lld:pubmed |
| pubmed-article:8240107 | pubmed:articleTitle | A new codon 15 rhodopsin gene mutation in autosomal dominant retinitis pigmentosa is associated with sectorial disease. | lld:pubmed |
| pubmed-article:8240107 | pubmed:affiliation | Department of Ophthalmology, University of Melbourne, Australia. | lld:pubmed |
| pubmed-article:8240107 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8240107 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:6010 | entrezgene:pubmed | pubmed-article:8240107 | lld:entrezgene |
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