Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B8718dbc4800dcb3539889d72e4fb67d2> ?p ?o ?g. }
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- B8718dbc4800dcb3539889d72e4fb67d2 hasDbXref "NCIT:C36407" @default.
- B8718dbc4800dcb3539889d72e4fb67d2 hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- B8718dbc4800dcb3539889d72e4fb67d2 hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- B8718dbc4800dcb3539889d72e4fb67d2 type Axiom @default.
- B8718dbc4800dcb3539889d72e4fb67d2 annotatedProperty IAO_0000115 @default.
- B8718dbc4800dcb3539889d72e4fb67d2 annotatedSource MONDO_0100398 @default.
- B8718dbc4800dcb3539889d72e4fb67d2 annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly inv(3)(q21.3;q26.2). (A cytogenetic abnormality that refers to a paracentric inversion involving breakpoints on the long (q23.1 and q26.2) of chromosome 3. It is associated with acute myeloid leukemia.)" @default.