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Q54319740-EF1BB2F5-661F-4D42-912E-0FAC991F78BE
Q54319740-EF1BB2F5-661F-4D42-912E-0FAC991F78BE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54319740-EF1BB2F5-661F-4D42-912E-0FAC991F78BE
A MID1 gene mutation in a patient with Opitz G/BBB syndrome that altered the 3D structure of SPRY domain.
P2860
Q54319740-EF1BB2F5-661F-4D42-912E-0FAC991F78BE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54319740-EF1BB2F5-661F-4D42-912E-0FAC991F78BE
rank
NormalRank
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Statement
wasDerivedFrom
d95f8f4fae98856fa434e97ddf04a07a6a91cb75
P2860
Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit alpha 4.