Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B60300c6c477a6a1cb2fa2ac9e6e691b3> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B60300c6c477a6a1cb2fa2ac9e6e691b3 NCIT_P378 "NCI" @default.
- B60300c6c477a6a1cb2fa2ac9e6e691b3 type Axiom @default.
- B60300c6c477a6a1cb2fa2ac9e6e691b3 annotatedProperty IAO_0000115 @default.
- B60300c6c477a6a1cb2fa2ac9e6e691b3 annotatedSource NCIT_C185461 @default.
- B60300c6c477a6a1cb2fa2ac9e6e691b3 annotatedTarget "A complex cytogenetic abnormality where one copy of chromosome 16 has undergone chromosomal rearrangement in the vicinity of 16p13.3, which is the region containing the 2 genes that encode hemoglobin subunit alpha (HBA; alpha-globin), HBA1 and HBA2. This rearrangement results in amplification of a 3.7 kb fragment containing of one of the HBA genes (usually HBA2) and may lead to simultaneous deletion of the other HBA gene (usually HBA1)." @default.