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Q24338418-2BA46D14-3188-488A-BE0B-95BCCE64F9DC
Q24338418-2BA46D14-3188-488A-BE0B-95BCCE64F9DC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24338418-2BA46D14-3188-488A-BE0B-95BCCE64F9DC
Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells
P2860
Q24338418-2BA46D14-3188-488A-BE0B-95BCCE64F9DC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24338418-2BA46D14-3188-488A-BE0B-95BCCE64F9DC
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
a8e129d383bd1c67f2f15ec75be8a0d0f1b294bf
P2860
Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene