Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C140243> ?p ?o ?g. }
Showing items 1 to 57 of
57
with 100 items per page.
- NCIT_C140243 IAO_0000115 "Human BSND wild-type allele is located in the vicinity of 1p32.3 and is approximately 12 kb in length. This allele, which encodes Barttin protein, plays a role in the modulation of chloride transport. Mutation of the gene is associated with Bartter syndrome with sensorineural deafness." @default.
- NCIT_C140243 NCIT_NHC0 "C140243" @default.
- NCIT_C140243 NCIT_P100 "606412" @default.
- NCIT_C140243 NCIT_P102 "AY034632" @default.
- NCIT_C140243 NCIT_P106 "Gene or Genome" @default.
- NCIT_C140243 NCIT_P108 "BSND wt Allele" @default.
- NCIT_C140243 NCIT_P208 "CL538402" @default.
- NCIT_C140243 NCIT_P321 "7809" @default.
- NCIT_C140243 NCIT_R37 NCIT_C17710 @default.
- NCIT_C140243 NCIT_R37 NCIT_C17828 @default.
- NCIT_C140243 NCIT_R37 NCIT_C18219 @default.
- NCIT_C140243 NCIT_R37 NCIT_C19950 @default.
- NCIT_C140243 NCIT_R37 NCIT_C19986 @default.
- NCIT_C140243 NCIT_R37 NCIT_C20139 @default.
- NCIT_C140243 NCIT_R37 NCIT_C20480 @default.
- NCIT_C140243 NCIT_R37 NCIT_C21079 @default.
- NCIT_C140243 NCIT_R37 NCIT_C28498 @default.
- NCIT_C140243 NCIT_R37 NCIT_C40515 @default.
- NCIT_C140243 NCIT_R37 NCIT_C40792 @default.
- NCIT_C140243 NCIT_R40 NCIT_C12219 @default.
- NCIT_C140243 NCIT_R40 NCIT_C13282 @default.
- NCIT_C140243 NCIT_R40 NCIT_C13377 @default.
- NCIT_C140243 NCIT_R40 NCIT_C13432 @default.
- NCIT_C140243 NCIT_R40 NCIT_C13446 @default.
- NCIT_C140243 NCIT_R40 NCIT_C14135 @default.
- NCIT_C140243 NCIT_R40 NCIT_C24994 @default.
- NCIT_C140243 NCIT_R40 NCIT_C32221 @default.
- NCIT_C140243 NCIT_R40 NCIT_C34070 @default.
- NCIT_C140243 NCIT_R41 NCIT_C14182 @default.
- NCIT_C140243 NCIT_R41 NCIT_C14225 @default.
- NCIT_C140243 NCIT_R41 NCIT_C14234 @default.
- NCIT_C140243 NCIT_R41 NCIT_C14250 @default.
- NCIT_C140243 NCIT_R41 NCIT_C14262 @default.
- NCIT_C140243 NCIT_R41 NCIT_C14282 @default.
- NCIT_C140243 NCIT_R41 NCIT_C25796 @default.
- NCIT_C140243 NCIT_R41 NCIT_C79740 @default.
- NCIT_C140243 normalizedInformationContent "100" @default.
- NCIT_C140243 referenceCount "1" @default.
- NCIT_C140243 hasExactSynonym "BART" @default.
- NCIT_C140243 hasExactSynonym "BSND wt Allele" @default.
- NCIT_C140243 hasExactSynonym "Bartter Syndrome, Infantile, With Sensorineural Deafness (Barttin) 2 Gene" @default.
- NCIT_C140243 hasExactSynonym "Barttin CLCNK Type Accessory Beta Subunit wt Allele" @default.
- NCIT_C140243 hasExactSynonym "DFNB73" @default.
- NCIT_C140243 hasExactSynonym "Deafness, Autosomal Recessive 73 Gene" @default.
- NCIT_C140243 type Class @default.
- NCIT_C140243 isDefinedBy ncit.owl @default.
- NCIT_C140243 label "BSND wt Allele" @default.
- NCIT_C140243 subClassOf B3c54d318bbf7783ee896f9f86a5299ac @default.
- NCIT_C140243 subClassOf B4ee1cb4f04c5d562a2592881c21b5c70 @default.
- NCIT_C140243 subClassOf NCIT_C140242 @default.
- NCIT_C140243 subClassOf NCIT_C140243 @default.
- NCIT_C140243 subClassOf NCIT_C16612 @default.
- NCIT_C140243 subClassOf NCIT_C21295 @default.
- NCIT_C140243 subClassOf NCIT_C25869 @default.
- NCIT_C140243 subClassOf NCIT_C25993 @default.
- NCIT_C140243 subClassOf NCIT_C26039 @default.
- NCIT_C140243 subClassOf NCIT_C28533 @default.