Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B96a63167689b6b82903cd4a467dfa315> ?p ?o ?g. }
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- B96a63167689b6b82903cd4a467dfa315 hasDbXref "MESH:D017496" @default.
- B96a63167689b6b82903cd4a467dfa315 type Axiom @default.
- B96a63167689b6b82903cd4a467dfa315 annotatedProperty IAO_0000115 @default.
- B96a63167689b6b82903cd4a467dfa315 annotatedSource MONDO_0019290 @default.
- B96a63167689b6b82903cd4a467dfa315 annotatedTarget "A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections." @default.