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- NCIT_C52268 IAO_0000115 "Human SEM1 wild-type allele is located in the vicinity of 7q21.3 and is approximately 228 kb in length. This allele, which encodes 26 proteasome complex subunit SEM1 protein, is involved in the mediation of protein degradation. The gene may play a role in split hand/split foot malformation." @default.
- NCIT_C52268 NCIT_NHC0 "C52268" @default.
- NCIT_C52268 NCIT_P100 "601285" @default.
- NCIT_C52268 NCIT_P101 "DSS1/SEM1 Family" @default.
- NCIT_C52268 NCIT_P102 "U41515" @default.
- NCIT_C52268 NCIT_P106 "Gene or Genome" @default.
- NCIT_C52268 NCIT_P107 "SEM1 wt Allele" @default.
- NCIT_C52268 NCIT_P108 "SEM1 wt Allele" @default.
- NCIT_C52268 NCIT_P207 "C1705135" @default.
- NCIT_C52268 NCIT_P211 "biological_process unknown" @default.
- NCIT_C52268 NCIT_P211 "cellular_component unknown" @default.
- NCIT_C52268 NCIT_P211 "molecular_function unknown" @default.
- NCIT_C52268 NCIT_P321 "7979" @default.
- NCIT_C52268 NCIT_P322 "CTRP" @default.
- NCIT_C52268 NCIT_P366 "SHFM1_wt_Allele" @default.
- NCIT_C52268 NCIT_P96 "Deleted in Split Hand/Split Foot Protein 1" @default.
- NCIT_C52268 NCIT_R130 NCIT_C18611 @default.
- NCIT_C52268 NCIT_R130 NCIT_C20633 @default.
- NCIT_C52268 NCIT_R130 NCIT_C39702 @default.
- NCIT_C52268 NCIT_R130 NCIT_C39705 @default.
- NCIT_C52268 NCIT_R130 NCIT_C91483 @default.
- NCIT_C52268 NCIT_R130 NCIT_C91521 @default.
- NCIT_C52268 NCIT_R37 NCIT_C16397 @default.
- NCIT_C52268 NCIT_R37 NCIT_C17710 @default.
- NCIT_C52268 NCIT_R37 NCIT_C17729 @default.
- NCIT_C52268 NCIT_R37 NCIT_C17828 @default.
- NCIT_C52268 NCIT_R37 NCIT_C18104 @default.
- NCIT_C52268 NCIT_R37 NCIT_C18219 @default.
- NCIT_C52268 NCIT_R37 NCIT_C18469 @default.
- NCIT_C52268 NCIT_R37 NCIT_C19406 @default.
- NCIT_C52268 NCIT_R37 NCIT_C19536 @default.
- NCIT_C52268 NCIT_R37 NCIT_C19903 @default.
- NCIT_C52268 NCIT_R37 NCIT_C19946 @default.
- NCIT_C52268 NCIT_R37 NCIT_C19986 @default.
- NCIT_C52268 NCIT_R37 NCIT_C20480 @default.
- NCIT_C52268 NCIT_R37 NCIT_C21102 @default.
- NCIT_C52268 NCIT_R37 NCIT_C21124 @default.
- NCIT_C52268 NCIT_R37 NCIT_C21147 @default.
- NCIT_C52268 NCIT_R37 NCIT_C21198 @default.
- NCIT_C52268 NCIT_R37 NCIT_C28498 @default.
- NCIT_C52268 NCIT_R37 NCIT_C61559 @default.
- NCIT_C52268 NCIT_R40 NCIT_C12219 @default.
- NCIT_C52268 NCIT_R40 NCIT_C13282 @default.
- NCIT_C52268 NCIT_R40 NCIT_C13377 @default.
- NCIT_C52268 NCIT_R40 NCIT_C13432 @default.
- NCIT_C52268 NCIT_R40 NCIT_C13446 @default.
- NCIT_C52268 NCIT_R40 NCIT_C13771 @default.
- NCIT_C52268 NCIT_R40 NCIT_C14135 @default.
- NCIT_C52268 NCIT_R40 NCIT_C32221 @default.
- NCIT_C52268 NCIT_R40 NCIT_C34070 @default.
- NCIT_C52268 NCIT_R41 NCIT_C14182 @default.
- NCIT_C52268 NCIT_R41 NCIT_C14225 @default.
- NCIT_C52268 NCIT_R41 NCIT_C14234 @default.
- NCIT_C52268 NCIT_R41 NCIT_C14250 @default.
- NCIT_C52268 NCIT_R41 NCIT_C14262 @default.
- NCIT_C52268 NCIT_R41 NCIT_C14282 @default.
- NCIT_C52268 NCIT_R41 NCIT_C25796 @default.
- NCIT_C52268 NCIT_R41 NCIT_C79740 @default.
- NCIT_C52268 normalizedInformationContent "100" @default.
- NCIT_C52268 referenceCount "1" @default.
- NCIT_C52268 hasExactSynonym "C7orf76" @default.
- NCIT_C52268 hasExactSynonym "Chromosome 7 Open Reading Frame 76 Gene" @default.
- NCIT_C52268 hasExactSynonym "DSS1" @default.
- NCIT_C52268 hasExactSynonym "Deleted In Split-Hand/Split-Foot 1 Gene" @default.
- NCIT_C52268 hasExactSynonym "Deleted In Split-Hand/Split-Foot 1 Region" @default.
- NCIT_C52268 hasExactSynonym "Deleted in Split-Hand/Foot 1 Gene" @default.
- NCIT_C52268 hasExactSynonym "Deleted in Split-Hand/Split-Foot 1 Region Gene" @default.
- NCIT_C52268 hasExactSynonym "ECD" @default.
- NCIT_C52268 hasExactSynonym "FLJ42280" @default.
- NCIT_C52268 hasExactSynonym "SEM1 26S Proteasome Complex Subunit wt Allele" @default.
- NCIT_C52268 hasExactSynonym "SEM1 wt Allele" @default.
- NCIT_C52268 hasExactSynonym "SEM1, 26S Proteasome Complex Subunit Gene" @default.
- NCIT_C52268 hasExactSynonym "SHFD1" @default.
- NCIT_C52268 hasExactSynonym "SHFDG1" @default.
- NCIT_C52268 hasExactSynonym "SHFM1" @default.
- NCIT_C52268 hasExactSynonym "SHSF1" @default.
- NCIT_C52268 hasExactSynonym "Shfdg1" @default.
- NCIT_C52268 hasExactSynonym "Split Hand/Foot Malformation (Ectrodactyly) Type 1 Gene" @default.
- NCIT_C52268 inSubset NCIT_C116977 @default.
- NCIT_C52268 inSubset NCIT_C142799 @default.
- NCIT_C52268 inSubset NCIT_C142800 @default.
- NCIT_C52268 type Class @default.
- NCIT_C52268 isDefinedBy ncit.owl @default.
- NCIT_C52268 label "SEM1 wt Allele" @default.
- NCIT_C52268 subClassOf NCIT_C16612 @default.
- NCIT_C52268 subClassOf NCIT_C20194 @default.
- NCIT_C52268 subClassOf NCIT_C20916 @default.
- NCIT_C52268 subClassOf NCIT_C52268 @default.
- NCIT_C52268 equivalentClass B395c141269c015e329c3e17d3862193b @default.
- NCIT_C52268 equivalentClass Bf8b4b1bc8e5ca9c6cae619462bffd675 @default.