Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B41bb3c9c138c7ef0a4a06f0df4b1b5d5> ?p ?o ?g. }
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- B41bb3c9c138c7ef0a4a06f0df4b1b5d5 hasDbXref "Orphanet:636" @default.
- B41bb3c9c138c7ef0a4a06f0df4b1b5d5 hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B41bb3c9c138c7ef0a4a06f0df4b1b5d5 type Axiom @default.
- B41bb3c9c138c7ef0a4a06f0df4b1b5d5 annotatedProperty IAO_0000115 @default.
- B41bb3c9c138c7ef0a4a06f0df4b1b5d5 annotatedSource MONDO_0018975 @default.
- B41bb3c9c138c7ef0a4a06f0df4b1b5d5 annotatedTarget "A clinically heterogeneous, neurocutaneous genetic disorder characterized by cafe-au-lait spots, iris Lisch nodules, axillary and inguinal freckling, and multiple neurofibromas." @default.