Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bcc867ea0e07af6972b7f325d8e1f1671> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bcc867ea0e07af6972b7f325d8e1f1671 hasDbXref "Orphanet:90039" @default.
- Bcc867ea0e07af6972b7f325d8e1f1671 type Axiom @default.
- Bcc867ea0e07af6972b7f325d8e1f1671 annotatedProperty IAO_0000115 @default.
- Bcc867ea0e07af6972b7f325d8e1f1671 annotatedSource MONDO_0019537 @default.
- Bcc867ea0e07af6972b7f325d8e1f1671 annotatedTarget "Hemoglobin D disease(HbD) is a hemoglobinopathy characterized by production of abnormal variant hemoglobin known as hemoglobin D, with no or mild clinical manifestations (splenomegaly, very mild anemia)." @default.