Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B096eeefcf26645151bbbbb988a3291d9> ?p ?o ?g. }
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- B096eeefcf26645151bbbbb988a3291d9 hasDbXref "MONDO:nv" @default.
- B096eeefcf26645151bbbbb988a3291d9 hasDbXref "PMID:16026838" @default.
- B096eeefcf26645151bbbbb988a3291d9 hasDbXref "PMID:20930072" @default.
- B096eeefcf26645151bbbbb988a3291d9 type Axiom @default.
- B096eeefcf26645151bbbbb988a3291d9 annotatedProperty IAO_0000115 @default.
- B096eeefcf26645151bbbbb988a3291d9 annotatedSource MONDO_0003832 @default.
- B096eeefcf26645151bbbbb988a3291d9 annotatedTarget "A genetic deficiency of any of the component of the complement system (including the classical, alternative, and terminal pathway components), that can either be acquired or inherited." @default.