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Q41055576-F42E1638-48B2-416C-AEFA-2F11947467F7
Q41055576-F42E1638-48B2-416C-AEFA-2F11947467F7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41055576-F42E1638-48B2-416C-AEFA-2F11947467F7
Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita.
P2093
Q41055576-F42E1638-48B2-416C-AEFA-2F11947467F7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41055576-F42E1638-48B2-416C-AEFA-2F11947467F7
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
66d7b7288677e449ec7267fd38581ec867e9e73b
P1545
8
http://www.w3.org/2001/XMLSchema#string
P2093
H N Baris
http://www.w3.org/2001/XMLSchema#string