pubmed-article:21288980 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21288980 | lifeskim:mentions | umls-concept:C0008059 | lld:lifeskim |
pubmed-article:21288980 | lifeskim:mentions | umls-concept:C0011304 | lld:lifeskim |
pubmed-article:21288980 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:21288980 | lifeskim:mentions | umls-concept:C0012929 | lld:lifeskim |
pubmed-article:21288980 | lifeskim:mentions | umls-concept:C0439661 | lld:lifeskim |
pubmed-article:21288980 | lifeskim:mentions | umls-concept:C0205099 | lld:lifeskim |
pubmed-article:21288980 | pubmed:issue | 9 | lld:pubmed |
pubmed-article:21288980 | pubmed:dateCreated | 2011-3-1 | lld:pubmed |
pubmed-article:21288980 | pubmed:abstractText | We investigated mitochondrial DNA (mtDNA) variants in children with a first episode of acquired demyelinating syndromes (PD-ADS) of the CNS and their relationship to disease phenotype, including subsequent diagnosis of multiple sclerosis (MS). | lld:pubmed |
pubmed-article:21288980 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21288980 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21288980 | pubmed:language | eng | lld:pubmed |
pubmed-article:21288980 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21288980 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:21288980 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21288980 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:21288980 | pubmed:month | Mar | lld:pubmed |
pubmed-article:21288980 | pubmed:issn | 1526-632X | lld:pubmed |
pubmed-article:21288980 | pubmed:author | pubmed-author:ArnoldD LDL | lld:pubmed |
pubmed-article:21288980 | pubmed:author | pubmed-author:SadovnickA... | lld:pubmed |
pubmed-article:21288980 | pubmed:author | pubmed-author:Venkateswaran... | lld:pubmed |
pubmed-article:21288980 | pubmed:author | pubmed-author:GagneDD | lld:pubmed |
pubmed-article:21288980 | pubmed:author | pubmed-author:SimonD KDK | lld:pubmed |
pubmed-article:21288980 | pubmed:author | pubmed-author:ZhengKK | lld:pubmed |
pubmed-article:21288980 | pubmed:author | pubmed-author:Bar-OrAA | lld:pubmed |
pubmed-article:21288980 | pubmed:author | pubmed-author:SchererS WSW | lld:pubmed |
pubmed-article:21288980 | pubmed:author | pubmed-author:SacchettiMM | lld:pubmed |
pubmed-article:21288980 | pubmed:author | pubmed-author:BanwellBB | lld:pubmed |
pubmed-article:21288980 | pubmed:author | pubmed-author:Canadian... | lld:pubmed |
pubmed-article:21288980 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:21288980 | pubmed:day | 1 | lld:pubmed |
pubmed-article:21288980 | pubmed:volume | 76 | lld:pubmed |
pubmed-article:21288980 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:21288980 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:21288980 | pubmed:pagination | 774-80 | lld:pubmed |
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pubmed-article:21288980 | pubmed:year | 2011 | lld:pubmed |
pubmed-article:21288980 | pubmed:articleTitle | Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination. | lld:pubmed |
pubmed-article:21288980 | pubmed:affiliation | Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02215, USA. | lld:pubmed |
pubmed-article:21288980 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:21288980 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:21288980 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:21288980 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:21288980 | lld:pubmed |