Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B56a7914d2c731d1cb919ba55c3ea131f> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B56a7914d2c731d1cb919ba55c3ea131f NCIT_P378 "NICHD" @default.
- B56a7914d2c731d1cb919ba55c3ea131f type Axiom @default.
- B56a7914d2c731d1cb919ba55c3ea131f annotatedProperty NCIT_P325 @default.
- B56a7914d2c731d1cb919ba55c3ea131f annotatedSource NCIT_C35344 @default.
- B56a7914d2c731d1cb919ba55c3ea131f annotatedTarget "An autosomal recessive disorder resulting from the production of hemoglobin D, secondary to various substitution mutations in the beta chain, and characterized by mild hemolytic anemia and possible splenomegaly. Multiple subtypes of hemoglobin D have been identified." @default.