Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bfefcfd3ffa26dc9de7ebb61f441aabc6> ?p ?o ?g. }
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- Bfefcfd3ffa26dc9de7ebb61f441aabc6 hasDbXref "NCIT:C36499" @default.
- Bfefcfd3ffa26dc9de7ebb61f441aabc6 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- Bfefcfd3ffa26dc9de7ebb61f441aabc6 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- Bfefcfd3ffa26dc9de7ebb61f441aabc6 type Axiom @default.
- Bfefcfd3ffa26dc9de7ebb61f441aabc6 annotatedProperty IAO_0000115 @default.
- Bfefcfd3ffa26dc9de7ebb61f441aabc6 annotatedSource MONDO_0100403 @default.
- Bfefcfd3ffa26dc9de7ebb61f441aabc6 annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly loss of chromosome 17p. (A cytogenetic abnormality that refers to the loss of all or part of the short arm of chromosome 17 (17p).)" @default.