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Q35196805-81A13437-B891-4665-8C2B-2019FCFC6C5A
Q35196805-81A13437-B891-4665-8C2B-2019FCFC6C5A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35196805-81A13437-B891-4665-8C2B-2019FCFC6C5A
Finnish type of familial amyloidosis: cosegregation of Asp187----Asn mutation of gelsolin with the disease in three large families.
P2860
Q35196805-81A13437-B891-4665-8C2B-2019FCFC6C5A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35196805-81A13437-B891-4665-8C2B-2019FCFC6C5A
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
c801830f861fbfbd8294935b5e41511f7d29ae19
P2860
An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.