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Q50318604-3C86E120-C421-489F-B7AE-3027F8FF2238
Q50318604-3C86E120-C421-489F-B7AE-3027F8FF2238
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50318604-3C86E120-C421-489F-B7AE-3027F8FF2238
Whole-exome sequencing identifies novel variants in PNPT1 causing oxidative phosphorylation defects and severe multisystem disease.
P698
Q50318604-3C86E120-C421-489F-B7AE-3027F8FF2238
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50318604-3C86E120-C421-489F-B7AE-3027F8FF2238
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
44c871cc6bb6e16ef7288c91584651149e0815fd
P698
27759031
http://www.w3.org/2001/XMLSchema#string