Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C51544> ?p ?o ?g. }
- NCIT_C51544 IAO_0000115 "Human FGFR3 wild-type allele is located in the vicinity of 4p16.3 and is approximately 15 kb in length. This allele, which encodes fibroblast growth factor receptor 3 protein, is involved in mitogenesis, differentiation, and bone development and maintenance. Alterations in the gene resulting in defects cause, achondroplasia, crouzon syndrome, thanatophoric dysplasia, coronal synostosis, hypochondroplasia, bladder and cervix cancers." @default.
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- NCIT_C51544 NCIT_P106 "Gene or Genome" @default.
- NCIT_C51544 NCIT_P107 "FGFR3 wt Allele" @default.
- NCIT_C51544 NCIT_P108 "FGFR3 wt Allele" @default.
- NCIT_C51544 NCIT_P207 "C1705145" @default.
- NCIT_C51544 NCIT_P211 "FGF receptor signaling pathway" @default.
- NCIT_C51544 NCIT_P211 "JAK-STAT cascade" @default.
- NCIT_C51544 NCIT_P211 "MAPKKK cascade" @default.
- NCIT_C51544 NCIT_P211 "cell growth" @default.
- NCIT_C51544 NCIT_P211 "fibroblast growth factor receptor activity" @default.
- NCIT_C51544 NCIT_P211 "integral to membrane" @default.
- NCIT_C51544 NCIT_P211 "integral to plasma membrane" @default.
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- NCIT_C51544 hasExactSynonym "ACH" @default.
- NCIT_C51544 hasExactSynonym "Achondroplasia, Thanatophoric Dwarfism Gene" @default.