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- NCIT_C156971 IAO_0000115 "Human CLN3 wild-type allele is located in the vicinity of 16p12.1 and is approximately 29 kb in length. This allele, which encodes battenin protein, is involved in microtubule-dependent transport of organelles. Deletions within the gene are associated with neuronal ceroid lipofuscinosis type 3 (Batten disease)." @default.
- NCIT_C156971 NCIT_NHC0 "C156971" @default.
- NCIT_C156971 NCIT_P100 "607042" @default.
- NCIT_C156971 NCIT_P102 "U32680" @default.
- NCIT_C156971 NCIT_P106 "Gene or Genome" @default.
- NCIT_C156971 NCIT_P108 "CLN3 wt Allele" @default.
- NCIT_C156971 NCIT_P208 "CL936053" @default.
- NCIT_C156971 NCIT_P321 "1201" @default.
- NCIT_C156971 NCIT_R130 NCIT_C18611 @default.
- NCIT_C156971 NCIT_R130 NCIT_C20633 @default.
- NCIT_C156971 NCIT_R130 NCIT_C39702 @default.
- NCIT_C156971 NCIT_R130 NCIT_C91440 @default.
- NCIT_C156971 NCIT_R37 NCIT_C17710 @default.
- NCIT_C156971 NCIT_R37 NCIT_C17828 @default.
- NCIT_C156971 NCIT_R37 NCIT_C18146 @default.
- NCIT_C156971 NCIT_R37 NCIT_C18219 @default.
- NCIT_C156971 NCIT_R37 NCIT_C19986 @default.
- NCIT_C156971 NCIT_R37 NCIT_C20139 @default.
- NCIT_C156971 NCIT_R37 NCIT_C21079 @default.
- NCIT_C156971 NCIT_R37 NCIT_C28498 @default.
- NCIT_C156971 NCIT_R40 NCIT_C12219 @default.
- NCIT_C156971 NCIT_R40 NCIT_C13282 @default.
- NCIT_C156971 NCIT_R40 NCIT_C13377 @default.
- NCIT_C156971 NCIT_R40 NCIT_C13432 @default.
- NCIT_C156971 NCIT_R40 NCIT_C13446 @default.
- NCIT_C156971 NCIT_R40 NCIT_C14135 @default.
- NCIT_C156971 NCIT_R40 NCIT_C26005 @default.
- NCIT_C156971 NCIT_R40 NCIT_C32221 @default.
- NCIT_C156971 NCIT_R40 NCIT_C34070 @default.
- NCIT_C156971 NCIT_R41 NCIT_C14182 @default.
- NCIT_C156971 NCIT_R41 NCIT_C14225 @default.
- NCIT_C156971 NCIT_R41 NCIT_C14234 @default.
- NCIT_C156971 NCIT_R41 NCIT_C14250 @default.
- NCIT_C156971 NCIT_R41 NCIT_C14262 @default.
- NCIT_C156971 NCIT_R41 NCIT_C14282 @default.
- NCIT_C156971 NCIT_R41 NCIT_C25796 @default.
- NCIT_C156971 NCIT_R41 NCIT_C79740 @default.
- NCIT_C156971 normalizedInformationContent "100" @default.
- NCIT_C156971 referenceCount "1" @default.
- NCIT_C156971 hasExactSynonym "BTN1" @default.
- NCIT_C156971 hasExactSynonym "BTS" @default.
- NCIT_C156971 hasExactSynonym "Batten, Spielmeyer-Vogt Disease Gene" @default.
- NCIT_C156971 hasExactSynonym "CLN3 wt Allele" @default.
- NCIT_C156971 hasExactSynonym "CLN3, Battenin wt Allele" @default.
- NCIT_C156971 hasExactSynonym "Ceroid-Lipofuscinosis, Neuronal 3 Gene" @default.
- NCIT_C156971 hasExactSynonym "JNCL" @default.
- NCIT_C156971 hasExactSynonym "Juvenile Neuronal Ceroid Lipofuscinosis Gene" @default.
- NCIT_C156971 type Class @default.
- NCIT_C156971 isDefinedBy ncit.owl @default.
- NCIT_C156971 label "CLN3 wt Allele" @default.
- NCIT_C156971 subClassOf B0f79b31b627d3dde762ee7b7b3e77e2d @default.
- NCIT_C156971 subClassOf B10389d969b086ef29db780af067f9cfc @default.
- NCIT_C156971 subClassOf B336fc732e871c6cd0287bbb4555ee952 @default.
- NCIT_C156971 subClassOf B5d0239a2919ad747e86c7ff6430538c3 @default.
- NCIT_C156971 subClassOf NCIT_C156970 @default.
- NCIT_C156971 subClassOf NCIT_C156971 @default.
- NCIT_C156971 subClassOf NCIT_C16612 @default.
- NCIT_C156971 subClassOf NCIT_C21295 @default.
- NCIT_C156971 subClassOf NCIT_C26006 @default.
- NCIT_C156971 subClassOf NCIT_C28533 @default.