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- NCIT_C101659 IAO_0000115 "Human TMEM138 wild-type allele is located in the vicinity of 11q12.2 and is approximately 8 kb in length. This allele, which encodes transmembrane protein 138, is involved in ciliogenesis." @default.
- NCIT_C101659 NCIT_NHC0 "C101659" @default.
- NCIT_C101659 NCIT_P100 "614459" @default.
- NCIT_C101659 NCIT_P102 "AF151030" @default.
- NCIT_C101659 NCIT_P106 "Gene or Genome" @default.
- NCIT_C101659 NCIT_P108 "TMEM138 wt Allele" @default.
- NCIT_C101659 NCIT_P207 "C3542423" @default.
- NCIT_C101659 NCIT_P321 "51524" @default.
- NCIT_C101659 NCIT_P98 "Mutation of the TMEM138 gene may be associated with Joubert syndrome type 2. (Science. 2012; 335:966-969.)" @default.
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- NCIT_C101659 normalizedInformationContent "100" @default.
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- NCIT_C101659 hasExactSynonym "HSPC196" @default.
- NCIT_C101659 hasExactSynonym "HSPC198" @default.
- NCIT_C101659 hasExactSynonym "JBTS16" @default.
- NCIT_C101659 hasExactSynonym "TMEM138 wt Allele" @default.
- NCIT_C101659 hasExactSynonym "Transmembrane Protein 138 wt Allele" @default.
- NCIT_C101659 type Class @default.
- NCIT_C101659 isDefinedBy ncit.owl @default.
- NCIT_C101659 label "TMEM138 wt Allele" @default.
- NCIT_C101659 subClassOf B11fe4d310f32dbbf8f65349df17a4ca9 @default.
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