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- NCIT_C156931 IAO_0000115 "Human METTL13 wild-type allele is located in the vicinity of 1q24.3 and is approximately 32 kb in length. This allele, which encodes eEF1A lysine and N-terminal methyltransferase protein, plays a role in the modulation of both apoptosis and protein translation. Mutation of the gene is associated with type 26 autosomal recessive deafness." @default.
- NCIT_C156931 NCIT_NHC0 "C156931" @default.
- NCIT_C156931 NCIT_P100 "617987" @default.
- NCIT_C156931 NCIT_P102 "AF132936" @default.
- NCIT_C156931 NCIT_P106 "Gene or Genome" @default.
- NCIT_C156931 NCIT_P108 "METTL13 wt Allele" @default.
- NCIT_C156931 NCIT_P208 "CL935950" @default.
- NCIT_C156931 NCIT_P321 "51603" @default.
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- NCIT_C156931 NCIT_R37 NCIT_C21049 @default.
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- NCIT_C156931 NCIT_R37 NCIT_C28498 @default.
- NCIT_C156931 NCIT_R37 NCIT_C30022 @default.
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- NCIT_C156931 NCIT_R37 NCIT_C40727 @default.
- NCIT_C156931 NCIT_R37 NCIT_C41515 @default.
- NCIT_C156931 NCIT_R37 NCIT_C51037 @default.
- NCIT_C156931 NCIT_R40 NCIT_C12219 @default.
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- NCIT_C156931 NCIT_R40 NCIT_C13432 @default.
- NCIT_C156931 NCIT_R40 NCIT_C13446 @default.
- NCIT_C156931 NCIT_R40 NCIT_C14135 @default.
- NCIT_C156931 NCIT_R40 NCIT_C32221 @default.
- NCIT_C156931 NCIT_R40 NCIT_C34070 @default.
- NCIT_C156931 NCIT_R40 NCIT_C82134 @default.
- NCIT_C156931 NCIT_R41 NCIT_C14182 @default.
- NCIT_C156931 NCIT_R41 NCIT_C14225 @default.
- NCIT_C156931 NCIT_R41 NCIT_C14234 @default.
- NCIT_C156931 NCIT_R41 NCIT_C14250 @default.
- NCIT_C156931 NCIT_R41 NCIT_C14262 @default.
- NCIT_C156931 NCIT_R41 NCIT_C14282 @default.
- NCIT_C156931 NCIT_R41 NCIT_C25796 @default.
- NCIT_C156931 NCIT_R41 NCIT_C79740 @default.
- NCIT_C156931 normalizedInformationContent "100" @default.
- NCIT_C156931 referenceCount "1" @default.
- NCIT_C156931 hasExactSynonym "5630401D24Rik" @default.
- NCIT_C156931 hasExactSynonym "CGI-01" @default.
- NCIT_C156931 hasExactSynonym "DFNB26" @default.
- NCIT_C156931 hasExactSynonym "DFNB26M" @default.
- NCIT_C156931 hasExactSynonym "DFNM1" @default.
- NCIT_C156931 hasExactSynonym "Deafness (Autosomal Recessive, Nonsyndromic) Modifier 1 Gene" @default.
- NCIT_C156931 hasExactSynonym "Deafness (Recessive, Non-Syndromic) Modifier 1 Gene" @default.
- NCIT_C156931 hasExactSynonym "Deafness (Recessive, Nonsyndromic) Modifier 1 Gene" @default.
- NCIT_C156931 hasExactSynonym "Deafness, Autosomal Recessive 26 Gene" @default.
- NCIT_C156931 hasExactSynonym "FEAT" @default.
- NCIT_C156931 hasExactSynonym "Faint Expression in Normal Tissues, Aberrant Overexpression in Tumors Gene" @default.
- NCIT_C156931 hasExactSynonym "KIAA0859" @default.
- NCIT_C156931 hasExactSynonym "METTL13 wt Allele" @default.
- NCIT_C156931 hasExactSynonym "METTL13" @default.
- NCIT_C156931 hasExactSynonym "Methyltransferase 13, eEF1A Lysine and N-Terminal Methyltransferase Gene" @default.
- NCIT_C156931 hasExactSynonym "Methyltransferase 13, eEF1A N-Terminus and K55 wt Allele" @default.
- NCIT_C156931 hasExactSynonym "Methyltransferase Like 13 Gene" @default.
- NCIT_C156931 hasExactSynonym "Methyltransferase-Like 13 Gene" @default.
- NCIT_C156931 hasExactSynonym "eEF1A Lysine and N-Terminal Methyltransferase Gene" @default.
- NCIT_C156931 hasExactSynonym "feat" @default.
- NCIT_C156931 type Class @default.
- NCIT_C156931 isDefinedBy ncit.owl @default.
- NCIT_C156931 label "METTL13 wt Allele" @default.
- NCIT_C156931 subClassOf B3044ed97826ae969a5c979b35fcb7741 @default.
- NCIT_C156931 subClassOf B613f2a9c1b8f6836e92e1c19e8b52ff4 @default.
- NCIT_C156931 subClassOf NCIT_C156930 @default.
- NCIT_C156931 subClassOf NCIT_C156931 @default.
- NCIT_C156931 subClassOf NCIT_C16612 @default.
- NCIT_C156931 subClassOf NCIT_C21281 @default.
- NCIT_C156931 subClassOf NCIT_C25870 @default.
- NCIT_C156931 subClassOf NCIT_C26110 @default.