Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B10f20199cb958ef1e99dbf7ae9878732> ?p ?o ?g. }
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- B10f20199cb958ef1e99dbf7ae9878732 NCIT_P378 "NCI" @default.
- B10f20199cb958ef1e99dbf7ae9878732 type Axiom @default.
- B10f20199cb958ef1e99dbf7ae9878732 annotatedProperty IAO_0000115 @default.
- B10f20199cb958ef1e99dbf7ae9878732 annotatedSource NCIT_C201103 @default.
- B10f20199cb958ef1e99dbf7ae9878732 annotatedTarget "Human ESPN wild-type allele is located in the vicinity of 1p36.31 and is approximately 37 kb in length. This allele, which encodes espin protein, plays a role in microvillus formation, function and maintenance in mechanosensory and chemosensory cells. Mutation of the gene is associated with type 1M Usher syndrome, autosomal recessive neurosensory deafness type 36 and autosomal dominant sensorineural deafness without vestibular involvement." @default.