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- B771c4ed286f1b5f018134a1b33c474e7 NCIT_P378 "NCI-GLOSS" @default.
- B771c4ed286f1b5f018134a1b33c474e7 type Axiom @default.
- B771c4ed286f1b5f018134a1b33c474e7 annotatedProperty NCIT_P325 @default.
- B771c4ed286f1b5f018134a1b33c474e7 annotatedSource NCIT_C27264 @default.
- B771c4ed286f1b5f018134a1b33c474e7 annotatedTarget "An inherited condition marked by the following: (1) one or more first- or second-degree relatives (parent, sibling, child, grandparent, grandchild, aunt, or uncle) with malignant melanoma; (2) many moles, some of which are atypical (asymmetrical, raised, and/or different shades of tan, brown, black, or red) and often of different sizes; and (3) moles that have specific features when examined under a microscope. FAMMM syndrome increases the risk of melanoma and may increase the risk of pancreatic cancer." @default.