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Q54977127-654C8277-D691-442B-9AA7-5A74F35DE8FC
Q54977127-654C8277-D691-442B-9AA7-5A74F35DE8FC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-654C8277-D691-442B-9AA7-5A74F35DE8FC
A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family.
P2860
Q54977127-654C8277-D691-442B-9AA7-5A74F35DE8FC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54977127-654C8277-D691-442B-9AA7-5A74F35DE8FC
rank
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type
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Statement
wasDerivedFrom
eada7336effc25426f074832c44b32c3ba913451
P2860
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC.