Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B99ddde2fdcfbf716b889a2fdc35f2f5c> ?p ?o ?g. }
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- B99ddde2fdcfbf716b889a2fdc35f2f5c NCIT_P378 "ACC/AHA" @default.
- B99ddde2fdcfbf716b889a2fdc35f2f5c type Axiom @default.
- B99ddde2fdcfbf716b889a2fdc35f2f5c annotatedProperty NCIT_P325 @default.
- B99ddde2fdcfbf716b889a2fdc35f2f5c annotatedSource NCIT_C36529 @default.
- B99ddde2fdcfbf716b889a2fdc35f2f5c annotatedTarget "A chromosomal abnormality consisting of the presence of part or all of a third copy of chromosome 13 in somatic cells." @default.