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Q51483708-642BA9A5-BC76-432E-A811-CFBDCBF99883
Q51483708-642BA9A5-BC76-432E-A811-CFBDCBF99883
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51483708-642BA9A5-BC76-432E-A811-CFBDCBF99883
Identification of a Novel Deletion Mutation (c.1780delG) and a Novel Splice-Site Mutation (c.1412-1G>A) in the CCM1/KRIT1 Gene Associated with Familial Cerebral Cavernous Malformation in the Chinese Population.
P2860
Q51483708-642BA9A5-BC76-432E-A811-CFBDCBF99883
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51483708-642BA9A5-BC76-432E-A811-CFBDCBF99883
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
d269b37d9509ce702381e221640173c3813a7aea
P2860
A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformations