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Q34476065-A621451B-62E0-4AFC-A467-0087767CEB5C
Q34476065-A621451B-62E0-4AFC-A467-0087767CEB5C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34476065-A621451B-62E0-4AFC-A467-0087767CEB5C
Meesmann corneal dystrophy (MECD): report of 2 families and a novel mutation in the cornea specific keratin 12 (KRT12) gene.
P2860
Q34476065-A621451B-62E0-4AFC-A467-0087767CEB5C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34476065-A621451B-62E0-4AFC-A467-0087767CEB5C
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
0edc576cb72d4d05540d96c10eed23d104ebfcb7
P2860
Human keratin diseases: hereditary fragility of specific epithelial tissues.