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764c5e9b5d7e6efda2b904dca65733daed2f6abe
764c5e9b5d7e6efda2b904dca65733daed2f6abe
Reference
http://www.wikidata.org/reference/764c5e9b5d7e6efda2b904dca65733daed2f6abe
Q21122498-3D3AA833-A029-4952-9AC5-9831A6D281AB
Q21122498-5B5A8495-1D57-43E3-88D2-255226C0145B
wasDerivedFrom
764c5e9b5d7e6efda2b904dca65733daed2f6abe
Reference
http://www.wikidata.org/reference/764c5e9b5d7e6efda2b904dca65733daed2f6abe
type
Reference
P1640
UniProt
P248
Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex
UniProt-GOA
P352
Q7Z412
http://www.w3.org/2001/XMLSchema#string
P459
IPI
P813
2019-05-09T00:00:00Z
http://www.w3.org/2001/XMLSchema#dateTime
P854
annotations?geneProductId=UniProtKB:Q7Z412
P352
Q7Z412
P813
fc5e1d4d543b33f61175b4ef633bd1d0