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- NCIT_C177165 IAO_0000115 "Human SOS2 wild-type allele is located in the vicinity of 14q21.3 and is approximately 114 kb in length. This allele, which encodes son of sevenless homolog 2 protein, is involved in the modulation of Ras signaling. Mutation of the gene is associated with Noonan syndrome 9." @default.
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- NCIT_C177165 NCIT_P106 "Gene or Genome" @default.
- NCIT_C177165 NCIT_P108 "SOS2 wt Allele" @default.
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- NCIT_C177165 hasExactSynonym "NS9" @default.
- NCIT_C177165 hasExactSynonym "SOS Ras/Rho Guanine Nucleotide Exchange Factor 2 wt Allele" @default.
- NCIT_C177165 hasExactSynonym "SOS-2" @default.
- NCIT_C177165 hasExactSynonym "SOS2 wt Allele" @default.
- NCIT_C177165 hasExactSynonym "Son of Sevenless (Drosophilia) Homolog 2 Gene" @default.
- NCIT_C177165 hasExactSynonym "Son of Sevenless Homolog 2 (Drosophila) Gene" @default.
- NCIT_C177165 hasExactSynonym "Son of Sevenless, Drosophilia, Homolog 2 Gene" @default.
- NCIT_C177165 type Class @default.
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- NCIT_C177165 label "SOS2 wt Allele" @default.
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