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- NCIT_C101656 IAO_0000115 "Human RGS4 wild-type allele is located in the vicinity of 1q23.3 and is approximately 8 kb in length. This allele, which encodes regulator of G-protein signaling 4 protein, plays a role in the modulation of G-protein signaling. Mutation of the gene may be associated with both schizophrenia and Parkinson disease." @default.
- NCIT_C101656 NCIT_NHC0 "C101656" @default.
- NCIT_C101656 NCIT_P100 "602516" @default.
- NCIT_C101656 NCIT_P102 "BC051869" @default.
- NCIT_C101656 NCIT_P106 "Gene or Genome" @default.
- NCIT_C101656 NCIT_P108 "RGS4 wt Allele" @default.
- NCIT_C101656 NCIT_P207 "C3538835" @default.
- NCIT_C101656 NCIT_P321 "5999" @default.
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- NCIT_C101656 normalizedInformationContent "100" @default.
- NCIT_C101656 referenceCount "1" @default.
- NCIT_C101656 hasExactSynonym "DKFZp761F1924" @default.
- NCIT_C101656 hasExactSynonym "MGC2124" @default.
- NCIT_C101656 hasExactSynonym "MGC60244" @default.
- NCIT_C101656 hasExactSynonym "RGP4" @default.
- NCIT_C101656 hasExactSynonym "RGS4 wt Allele" @default.
- NCIT_C101656 hasExactSynonym "RP11-430G6.1" @default.
- NCIT_C101656 hasExactSynonym "Regulator of G-Protein Signaling 4 wt Allele" @default.
- NCIT_C101656 hasExactSynonym "SCZD9" @default.
- NCIT_C101656 hasExactSynonym "Schizophrenia Disorder 9 Gene" @default.
- NCIT_C101656 type Class @default.
- NCIT_C101656 isDefinedBy ncit.owl @default.
- NCIT_C101656 label "RGS4 wt Allele" @default.
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- NCIT_C101656 subClassOf NCIT_C16612 @default.
- NCIT_C101656 subClassOf NCIT_C20921 @default.
- NCIT_C101656 subClassOf NCIT_C26048 @default.