Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Be9b51927c2a28cbc2b1e929d2c325b0c> ?p ?o ?g. }
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- Be9b51927c2a28cbc2b1e929d2c325b0c hasDbXref "NCIT:C131505" @default.
- Be9b51927c2a28cbc2b1e929d2c325b0c hasDbXref "https://orcid.org/0000-0001-9863-851X" @default.
- Be9b51927c2a28cbc2b1e929d2c325b0c hasDbXref "https://orcid.org/0000-0002-3302-4610" @default.
- Be9b51927c2a28cbc2b1e929d2c325b0c type Axiom @default.
- Be9b51927c2a28cbc2b1e929d2c325b0c annotatedProperty IAO_0000115 @default.
- Be9b51927c2a28cbc2b1e929d2c325b0c annotatedSource MONDO_0100407 @default.
- Be9b51927c2a28cbc2b1e929d2c325b0c annotatedTarget "Any acute myeloid leukemia that has the chromosomal anomaly t(11;15)(p15;q35). (A cytogenetic abnormality that refers to the translocation of chromosome 11p15 with chromosome 15q35. It results in the formation of NUP98/JARID1A fusion gene. It is associated with the development of acute myeloid leukemia with t(11;15)(p15;q35); NUP98-JARID1A.)" @default.