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e2205d0db398d1d25804f8ec619172b041ab3061
e2205d0db398d1d25804f8ec619172b041ab3061
Reference
http://www.wikidata.org/reference/e2205d0db398d1d25804f8ec619172b041ab3061
Q21132911-1AC998FA-7DC2-4191-A605-9C93281AC490
wasDerivedFrom
e2205d0db398d1d25804f8ec619172b041ab3061
Reference
http://www.wikidata.org/reference/e2205d0db398d1d25804f8ec619172b041ab3061
type
Reference
P1640
Proteome Inc.
P248
Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His----Tyr): complete structure of the normal human CA II gene
UniProt-GOA
P459
TAS
P813
2019-04-08T00:00:00Z
http://www.w3.org/2001/XMLSchema#dateTime
P854
annotations?geneProductId=UniProtKB:P00918
P813
b441aa14f32ad7a9e6fe04eb80002b4c