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- NCIT_C135730 IAO_0000115 "A nucleotide substitution at position 1476 of the coding sequence of the EGFR gene where cytosine has been mutated to adenine." @default.
- NCIT_C135730 NCIT_NHC0 "C135730" @default.
- NCIT_C135730 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C135730 NCIT_P107 "EGFR NM_005228.3:c.1476C>A" @default.
- NCIT_C135730 NCIT_P108 "EGFR NM_005228.3:c.1476C>A" @default.
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- NCIT_C135730 NCIT_P400 "376341" @default.
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- NCIT_C135730 hasExactSynonym "EGFR NM_005228.3:c.1476C>A" @default.
- NCIT_C135730 hasExactSynonym "EGFR S492R Gene Mutation" @default.
- NCIT_C135730 hasExactSynonym "EGFR c.1476C>A" @default.
- NCIT_C135730 hasExactSynonym "ERBB c.1476C>A" @default.
- NCIT_C135730 hasExactSynonym "ERBB1 c.1476C>A" @default.
- NCIT_C135730 hasExactSynonym "Epidermal Growth Factor Receptor Gene c.1476C>A" @default.
- NCIT_C135730 hasExactSynonym "HER1 c.1476C>A" @default.
- NCIT_C135730 hasExactSynonym "NM_005228.3:c.1476C>A" @default.
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- NCIT_C135730 inSubset NCIT_C142799 @default.
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- NCIT_C135730 label "EGFR NM_005228.3:c.1476C>A" @default.
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