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1
Q40492792-4ABD8208-75B5-4F7C-B1D1-037ABDDE9EFF
Q40492792-4ABD8208-75B5-4F7C-B1D1-037ABDDE9EFF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40492792-4ABD8208-75B5-4F7C-B1D1-037ABDDE9EFF
Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1.
P932
Q40492792-4ABD8208-75B5-4F7C-B1D1-037ABDDE9EFF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40492792-4ABD8208-75B5-4F7C-B1D1-037ABDDE9EFF
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
b06f60b609b6c7622a187eaec04e822fcf5fddba
P932
3260935
http://www.w3.org/2001/XMLSchema#string