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Q36247496-15F46523-1791-420D-A9F0-6E5CF06733C3
Q36247496-15F46523-1791-420D-A9F0-6E5CF06733C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36247496-15F46523-1791-420D-A9F0-6E5CF06733C3
Abnormal Paraplegin Expression in Swollen Neurites, τ- and α-Synuclein Pathology in a Case of Hereditary Spastic Paraplegia SPG7 with an Ala510Val Mutation
P2860
Q36247496-15F46523-1791-420D-A9F0-6E5CF06733C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36247496-15F46523-1791-420D-A9F0-6E5CF06733C3
rank
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type
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Statement
wasDerivedFrom
a6131efad6c80ac4a5bf061726daf3a5e2481dc9
P2860
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.