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Q47962206-12AFAF97-ACC4-48F5-9088-A27A401C8486
Q47962206-12AFAF97-ACC4-48F5-9088-A27A401C8486
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47962206-12AFAF97-ACC4-48F5-9088-A27A401C8486
Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome.
P2860
Q47962206-12AFAF97-ACC4-48F5-9088-A27A401C8486
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47962206-12AFAF97-ACC4-48F5-9088-A27A401C8486
rank
NormalRank
type
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Statement
wasDerivedFrom
03f366f62d2d323f35cea1636226c08a864a8129
P2860
Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatus