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Q46715449-48B9CE0F-12D2-4C1A-933C-CC983A0B95DF
Q46715449-48B9CE0F-12D2-4C1A-933C-CC983A0B95DF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46715449-48B9CE0F-12D2-4C1A-933C-CC983A0B95DF
Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress.
P2860
Q46715449-48B9CE0F-12D2-4C1A-933C-CC983A0B95DF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46715449-48B9CE0F-12D2-4C1A-933C-CC983A0B95DF
rank
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type
BestRank
Statement
wasDerivedFrom
152604a8e72d3b50ea59ef34a3a81fcd258ba3e9
P2860
A genetic and physiological study of impaired glucose homeostasis control in C57BL/6J mice.