Linked Life Data

20192983

Source:http://linkedlifedata.com/resource/pubmed/id/20192983

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2010-7-26
pubmed:abstractText
Sporadic inclusion body myositis (sIBM) is the most frequent acquired myopathy above the age of fifty. The exact mechanism causing this disease is not known, but immune-mediated features are prominent and are probably to play a role in its pathogenesis. TREX1 gene mutations are associated with a large range of autoimmune diseases, such as systemic lupus erythematosus. We investigated whether mutations in the TREX1 gene were associated with sIBM.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1468-1331
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1108-9
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
TREX1 mutations are not associated with sporadic inclusion body myositis.
pubmed:affiliation
Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands. f.cox@lumc.nl
pubmed:publicationType
Journal Article