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- NCIT_C82898 IAO_0000115 "Human MYT1L wild-type allele is located in the vicinity of 2p25.3 and is approximately 543 kb in length. This allele, which encodes myelin transcription factor 1-like protein, plays a role in both neuronal development and transcription. Genetic copy number variation is associated with schizophrenia." @default.
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- NCIT_C82898 NCIT_P106 "Gene or Genome" @default.
- NCIT_C82898 NCIT_P108 "MYT1L wt Allele" @default.
- NCIT_C82898 NCIT_P207 "C2826562" @default.
- NCIT_C82898 NCIT_P321 "23040" @default.
- NCIT_C82898 NCIT_P366 "MYT1L_wt_Allele" @default.
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- NCIT_C82898 hasExactSynonym "KIAA1106" @default.
- NCIT_C82898 hasExactSynonym "MYT1L wt Allele" @default.
- NCIT_C82898 hasExactSynonym "Myelin Transcription Factor 1-Like wt Allele" @default.
- NCIT_C82898 hasExactSynonym "NZF1" @default.
- NCIT_C82898 hasExactSynonym "Neural Zinc Finger Transcription Factor 1 Gene" @default.
- NCIT_C82898 type Class @default.
- NCIT_C82898 isDefinedBy ncit.owl @default.
- NCIT_C82898 label "MYT1L wt Allele" @default.
- NCIT_C82898 subClassOf Bb4d7840d5d677e431433283f7b192541 @default.
- NCIT_C82898 subClassOf Be5e978493d5410b805aef6118943fb7a @default.
- NCIT_C82898 subClassOf NCIT_C16612 @default.
- NCIT_C82898 subClassOf NCIT_C20420 @default.
- NCIT_C82898 subClassOf NCIT_C54362 @default.
- NCIT_C82898 subClassOf NCIT_C82897 @default.
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