| pubmed-article:12056939 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:12056939 | lifeskim:mentions | umls-concept:C0205494 | lld:lifeskim |
| pubmed-article:12056939 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:12056939 | lifeskim:mentions | umls-concept:C0012929 | lld:lifeskim |
| pubmed-article:12056939 | lifeskim:mentions | umls-concept:C0039082 | lld:lifeskim |
| pubmed-article:12056939 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:12056939 | lifeskim:mentions | umls-concept:C0439855 | lld:lifeskim |
| pubmed-article:12056939 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:12056939 | pubmed:dateCreated | 2002-6-11 | lld:pubmed |
| pubmed-article:12056939 | pubmed:abstractText | To confirm the pathogenicity of the G-to-A substitution at nucleotide 1606 (G1606A) mutation in the mitochondrial DNA (mtDNA) tRNA(Val) gene, and to characterize genotype-phenotype correlation. | lld:pubmed |
| pubmed-article:12056939 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12056939 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12056939 | pubmed:language | eng | lld:pubmed |
| pubmed-article:12056939 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12056939 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:12056939 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12056939 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12056939 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12056939 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12056939 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12056939 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:12056939 | pubmed:issn | 0003-9942 | lld:pubmed |
| pubmed-article:12056939 | pubmed:author | pubmed-author:BonillaEduard... | lld:pubmed |
| pubmed-article:12056939 | pubmed:author | pubmed-author:ShanskeSaraS | lld:pubmed |
| pubmed-article:12056939 | pubmed:author | pubmed-author:DiMauroSalvat... | lld:pubmed |
| pubmed-article:12056939 | pubmed:author | pubmed-author:SalviatiLeona... | lld:pubmed |
| pubmed-article:12056939 | pubmed:author | pubmed-author:SacconiSabrin... | lld:pubmed |
| pubmed-article:12056939 | pubmed:author | pubmed-author:GoochCliftonC | lld:pubmed |
| pubmed-article:12056939 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12056939 | pubmed:volume | 59 | lld:pubmed |
| pubmed-article:12056939 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12056939 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12056939 | pubmed:pagination | 1013-5 | lld:pubmed |
| pubmed-article:12056939 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:meshHeading | pubmed-meshheading:12056939... | lld:pubmed |
| pubmed-article:12056939 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:12056939 | pubmed:articleTitle | Complex neurologic syndrome associated with the G1606A mutation of mitochondrial DNA. | lld:pubmed |
| pubmed-article:12056939 | pubmed:affiliation | Department of Neurology, Columbia University, New York, NY, USA. | lld:pubmed |
| pubmed-article:12056939 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12056939 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:12056939 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:12056939 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:12056939 | lld:pubmed |
