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- NCIT_C92155 IAO_0000115 "Human MEF2A wild-type allele is located in the vicinity of 15q26 and is approximately 150 kb in length. This allele, which encodes myocyte-specific enhancer factor 2A protein, is involved in both myogenesis and growth factor or stress-stimulated transcriptional regulation." @default.
- NCIT_C92155 NCIT_NHC0 "C92155" @default.
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- NCIT_C92155 NCIT_P102 "NM_001130926" @default.
- NCIT_C92155 NCIT_P106 "Gene or Genome" @default.
- NCIT_C92155 NCIT_P108 "MEF2A wt Allele" @default.
- NCIT_C92155 NCIT_P207 "C2984880" @default.
- NCIT_C92155 NCIT_P321 "4205" @default.
- NCIT_C92155 NCIT_P98 "Mutation of the MEF2A gene may cause autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1). (EntrezGene)" @default.
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- NCIT_C92155 normalizedInformationContent "100" @default.
- NCIT_C92155 referenceCount "1" @default.
- NCIT_C92155 hasExactSynonym "ADCAD1" @default.
- NCIT_C92155 hasExactSynonym "MADS Box Transcription Enhancer Factor 2, Polypeptide A (Myocyte Enhancer Factor 2A) Gene" @default.
- NCIT_C92155 hasExactSynonym "MEF2A wt Allele" @default.
- NCIT_C92155 hasExactSynonym "Myocyte Enhancer Factor 2A wt Allele" @default.
- NCIT_C92155 hasExactSynonym "RSRFC4" @default.
- NCIT_C92155 hasExactSynonym "RSRFC9" @default.
- NCIT_C92155 type Class @default.
- NCIT_C92155 isDefinedBy ncit.owl @default.
- NCIT_C92155 label "MEF2A wt Allele" @default.
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