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Q28214525-D511CE36-AA76-494F-927C-4103D0B5F839
Q28214525-D511CE36-AA76-494F-927C-4103D0B5F839
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28214525-D511CE36-AA76-494F-927C-4103D0B5F839
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship
P2860
Q28214525-D511CE36-AA76-494F-927C-4103D0B5F839
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28214525-D511CE36-AA76-494F-927C-4103D0B5F839
rank
NormalRank
type
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Statement
wasDerivedFrom
82263779bf1da501a77073a1e3c40f62d9ccf80e
P2860
Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy.