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- NCIT_C101139 IAO_0000115 "A deletion of exons 2-7 of the EGFR gene corresponding to 804 nucleotides starting at position 334 through position 1137." @default.
- NCIT_C101139 NCIT_NHC0 "C101139" @default.
- NCIT_C101139 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C101139 NCIT_P107 "EGFR NM_005228.3:c.334_1137del804" @default.
- NCIT_C101139 NCIT_P108 "EGFR NM_005228.3:c.334_1137del804" @default.
- NCIT_C101139 NCIT_P207 "C3640004" @default.
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- NCIT_C101139 NCIT_R178 NCIT_C101140 @default.
- NCIT_C101139 NCIT_R178 NCIT_C3910 @default.
- NCIT_C101139 NCIT_R178 NCIT_C97926 @default.
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- NCIT_C101139 NCIT_R178 NCIT_C98356 @default.
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- NCIT_C101139 referenceCount "2" @default.
- NCIT_C101139 hasExactSynonym "EGFR NM_005228.3:c.334_1137del804" @default.
- NCIT_C101139 hasExactSynonym "EGFR c.334_1137del804" @default.
- NCIT_C101139 hasExactSynonym "EGFRvIII Extracellular Domain Mutation" @default.
- NCIT_C101139 hasExactSynonym "EGFRvIII Extracellular Domain Variant" @default.
- NCIT_C101139 hasExactSynonym "EGFRvIII Gene Mutation" @default.
- NCIT_C101139 hasExactSynonym "Epidermal Growth Factor Receptor Gene c.334_1137del804" @default.
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- NCIT_C101139 label "EGFR NM_005228.3:c.334_1137del804" @default.
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