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- NCIT_C185939 IAO_0000115 "A molecular genetic abnormality indicating the presence of a deletion mutation in exon 19 of the EGFR gene that results in constitutive epidermal growth factor receptor-dependent signal transduction and activation of downstream signaling pathways." @default.
- NCIT_C185939 NCIT_NHC0 "C185939" @default.
- NCIT_C185939 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C185939 NCIT_P107 "Activating EGFR Exon 19 Deletion Mutation" @default.
- NCIT_C185939 NCIT_P108 "Activating EGFR Exon 19 Deletion Mutation" @default.
- NCIT_C185939 NCIT_P208 "CL1778514" @default.
- NCIT_C185939 NCIT_P322 "CTRP" @default.
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- NCIT_C185939 NCIT_R177 NCIT_C21281 @default.
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- NCIT_C185939 NCIT_R177 NCIT_C25871 @default.
- NCIT_C185939 NCIT_R177 NCIT_C25872 @default.
- NCIT_C185939 NCIT_R178 NCIT_C3910 @default.
- NCIT_C185939 NCIT_R178 NCIT_C97926 @default.
- NCIT_C185939 NCIT_R178 NCIT_C97928 @default.
- NCIT_C185939 NCIT_R178 NCIT_C98356 @default.
- NCIT_C185939 normalizedInformationContent "100" @default.
- NCIT_C185939 referenceCount "1" @default.
- NCIT_C185939 hasExactSynonym "Activating EGFR Ex19Del Mutation" @default.
- NCIT_C185939 hasExactSynonym "Activating EGFR Exon 19 Deletion Mutation" @default.
- NCIT_C185939 hasExactSynonym "Activating EGFR Exon 19 Gene Deletion Mutation" @default.
- NCIT_C185939 hasExactSynonym "Activating ERBB Exon 19 Deletion Mutation" @default.
- NCIT_C185939 hasExactSynonym "Activating ERBB1 Exon 19 Deletion Mutation" @default.
- NCIT_C185939 hasExactSynonym "Activating Epidermal Growth Factor Receptor Exon 19 Deletion Mutation" @default.
- NCIT_C185939 hasExactSynonym "Activating Ex19Del Mutation" @default.
- NCIT_C185939 hasExactSynonym "Activating HER1 Exon 19 Deletion Mutation" @default.
- NCIT_C185939 hasExactSynonym "EGFR Exon 19 Activating Deletion Mutation" @default.
- NCIT_C185939 hasExactSynonym "EGFR Exon 19 Activating Gene Deletion Mutation" @default.
- NCIT_C185939 hasExactSynonym "Gain of Function EGFR Exon 19 Deletion Mutation" @default.
- NCIT_C185939 hasExactSynonym "Gain of Function EGFR Exon 19 Gene Deletion Mutation" @default.
- NCIT_C185939 inSubset NCIT_C116977 @default.
- NCIT_C185939 inSubset NCIT_C142799 @default.
- NCIT_C185939 inSubset NCIT_C142800 @default.
- NCIT_C185939 type Class @default.
- NCIT_C185939 isDefinedBy ncit.owl @default.
- NCIT_C185939 label "Activating EGFR Exon 19 Deletion Mutation" @default.
- NCIT_C185939 subClassOf NCIT_C126892 @default.
- NCIT_C185939 subClassOf NCIT_C128662 @default.
- NCIT_C185939 subClassOf NCIT_C141240 @default.
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- NCIT_C185939 subClassOf NCIT_C36327 @default.
- NCIT_C185939 subClassOf NCIT_C36391 @default.
- NCIT_C185939 subClassOf NCIT_C3910 @default.
- NCIT_C185939 subClassOf NCIT_C92172 @default.
- NCIT_C185939 subClassOf NCIT_C97926 @default.
- NCIT_C185939 subClassOf NCIT_C97927 @default.
- NCIT_C185939 subClassOf NCIT_C98357 @default.