Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B1120c44b0b282a561a14983b06ee44a0> ?p ?o ?g. }
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- B1120c44b0b282a561a14983b06ee44a0 hasDbXref "NCIT:C98898" @default.
- B1120c44b0b282a561a14983b06ee44a0 type Axiom @default.
- B1120c44b0b282a561a14983b06ee44a0 annotatedProperty IAO_0000115 @default.
- B1120c44b0b282a561a14983b06ee44a0 annotatedSource MONDO_0018963 @default.
- B1120c44b0b282a561a14983b06ee44a0 annotatedTarget "Methemoglobinemia inherited in an autosomal recessive pattern. It is caused by deficiency of the enzyme NADH methemoglobin reductase or the presence of abnormal hemoglobin M. It presents with cyanosis early in life. There is no evidence of cardiopulmonary disease present." @default.