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f5a937bb3b1b0bec3b8babc96d8af186f4c22381
f5a937bb3b1b0bec3b8babc96d8af186f4c22381
Reference
http://www.wikidata.org/reference/f5a937bb3b1b0bec3b8babc96d8af186f4c22381
Q21101107-D4EC6474-2EE0-4270-96C9-81297F7E2BDC
wasDerivedFrom
f5a937bb3b1b0bec3b8babc96d8af186f4c22381
Reference
http://www.wikidata.org/reference/f5a937bb3b1b0bec3b8babc96d8af186f4c22381
type
Reference
P1640
UniProt
P248
UniProt-GOA
A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy.
P352
O00429
http://www.w3.org/2001/XMLSchema#string
P459
IDA
P813
2019-04-08T00:00:00Z
http://www.w3.org/2001/XMLSchema#dateTime
P854
annotations?geneProductId=UniProtKB:O00429
P352
O00429
P813
b441aa14f32ad7a9e6fe04eb80002b4c