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- B5c40b45807b88339782dd416eebe0c63 NCIT_P378 "NCI" @default.
- B5c40b45807b88339782dd416eebe0c63 type Axiom @default.
- B5c40b45807b88339782dd416eebe0c63 annotatedProperty IAO_0000115 @default.
- B5c40b45807b88339782dd416eebe0c63 annotatedSource NCIT_C51542 @default.
- B5c40b45807b88339782dd416eebe0c63 annotatedTarget "Human FGFR1 wild-type allele is located within 8p11.2-p11.1 and is approximately 56 kb in length. This allele, which encodes basic fibroblast growth factor receptor 1 protein, is involved in the mediation of binding between both acidic and basic fibroblast growth factors and is involved in limb induction. Mutations in this gene are associated with several diseases, including Pfeiffer syndrome, Jackson-Weiss syndrome, Antley-Bixler syndrome, osteoglophonic dysplasia, and autosomal dominant Kallmann syndrome 2. Further, chromosomal aberrations involving the gene are associated with stem cell myeloproliferative disorder and stem cell leukemia lymphoma syndrome." @default.