Linked Life Data

20108429

Source:http://linkedlifedata.com/resource/pubmed/id/20108429

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2010-1-27
pubmed:databankReference
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1432-1203
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
127
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
117
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett Syndrome.
pubmed:affiliation
Genetics Unit, Department of Pediatrics, All India Institute of Medical Sciences, 110029, New Delhi, India. rajni.khajuria@gmail.com
pubmed:publicationType
Journal Article