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Q24672101-162D51CA-915F-49C9-98B4-CDF9134CBDFF
Q24672101-162D51CA-915F-49C9-98B4-CDF9134CBDFF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24672101-162D51CA-915F-49C9-98B4-CDF9134CBDFF
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome
P2860
Q24672101-162D51CA-915F-49C9-98B4-CDF9134CBDFF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24672101-162D51CA-915F-49C9-98B4-CDF9134CBDFF
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
aeb16120056258416028466f3fbfcc3d746e6e11
P2860
A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene