Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B2c318aae9febc22ba1f9a3e4ac74e8b7> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B2c318aae9febc22ba1f9a3e4ac74e8b7 NCIT_P378 "NCI" @default.
- B2c318aae9febc22ba1f9a3e4ac74e8b7 type Axiom @default.
- B2c318aae9febc22ba1f9a3e4ac74e8b7 annotatedProperty IAO_0000115 @default.
- B2c318aae9febc22ba1f9a3e4ac74e8b7 annotatedSource NCIT_C52261 @default.
- B2c318aae9febc22ba1f9a3e4ac74e8b7 annotatedTarget "Human WAS wild-type allele is located within Xp11.4-p11.21 and is approximately 8 kb in length. This allele, which encodes Wiskott-Aldrich syndrome protein, plays a role in actin cytoskeletal organization. Mutations in this gene are the cause of Wiskott-Aldrich syndrome an X-linked disease characterized by eczema, immune deficiencies and thrombocytopenia." @default.