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Q36626862-E1D4CBC9-ABF6-438F-AE16-C45EB40B8388
Q36626862-E1D4CBC9-ABF6-438F-AE16-C45EB40B8388
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36626862-E1D4CBC9-ABF6-438F-AE16-C45EB40B8388
Mutations in human DNA polymerase γ confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients.
P2860
Q36626862-E1D4CBC9-ABF6-438F-AE16-C45EB40B8388
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36626862-E1D4CBC9-ABF6-438F-AE16-C45EB40B8388
rank
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type
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Statement
wasDerivedFrom
ed1a1babec83f574168af527db19709b8a007d53
P2860
Disease mutations in the human mitochondrial DNA polymerase thumb subdomain impart severe defects in mitochondrial DNA replication.