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d106b989a53a73cda23f5956c509fa953350e0e7
d106b989a53a73cda23f5956c509fa953350e0e7
Reference
http://www.wikidata.org/reference/d106b989a53a73cda23f5956c509fa953350e0e7
Q21101107-872AA498-BE7A-42C6-9B70-18F002CA3AB2
Q21101107-C749FFA3-2748-4C09-A7B5-E7B644652ED0
wasDerivedFrom
d106b989a53a73cda23f5956c509fa953350e0e7
Reference
http://www.wikidata.org/reference/d106b989a53a73cda23f5956c509fa953350e0e7
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
IMP
P813
2019-04-08T00:00:00Z
http://www.w3.org/2001/XMLSchema#dateTime
P854
annotations?geneProductId=UniProtKB:O00429
P352
O00429
P813
b441aa14f32ad7a9e6fe04eb80002b4c