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Q43167089-6D0B8229-E024-4AC3-8B73-F33B7DA23BCE
Q43167089-6D0B8229-E024-4AC3-8B73-F33B7DA23BCE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43167089-6D0B8229-E024-4AC3-8B73-F33B7DA23BCE
Peroxisome deficiency causes a complex phenotype because of hepatic SREBP/Insig dysregulation associated with endoplasmic reticulum stress.
P2860
Q43167089-6D0B8229-E024-4AC3-8B73-F33B7DA23BCE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43167089-6D0B8229-E024-4AC3-8B73-F33B7DA23BCE
rank
NormalRank
type
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Statement
wasDerivedFrom
e8e3179b299d98c80618e4207ef35ef16c3876d3
P2860
Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder.