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- NCIT_C52505 IAO_0000115 "Human KRIT1 wild-type allele is located within 7q21-q22 and is approximately 102 kb in length. This allele, which encodes Krev interaction trapped protein 1, may play a role in integrin signaling modulation. Mutations in the gene, which encode for products that terminate prematurely, are a factor in familial cerebral cavernous malformations." @default.
- NCIT_C52505 NCIT_NHC0 "C52505" @default.
- NCIT_C52505 NCIT_P100 "604214" @default.
- NCIT_C52505 NCIT_P102 "NM_001013406" @default.
- NCIT_C52505 NCIT_P106 "Gene or Genome" @default.
- NCIT_C52505 NCIT_P108 "KRIT1 wt Allele" @default.
- NCIT_C52505 NCIT_P207 "C1706432" @default.
- NCIT_C52505 NCIT_P211 "small GTPase mediated signal transduction" @default.
- NCIT_C52505 NCIT_P211 "small GTPase regulatory/interacting protein activity" @default.
- NCIT_C52505 NCIT_P321 "889" @default.
- NCIT_C52505 NCIT_P366 "CCM1_wt_Allele" @default.
- NCIT_C52505 NCIT_P96 "Cerebral Cavernous Malformations 1" @default.
- NCIT_C52505 NCIT_R145 NCIT_C12219 @default.
- NCIT_C52505 NCIT_R145 NCIT_C21599 @default.
- NCIT_C52505 NCIT_R145 NCIT_C40342 @default.
- NCIT_C52505 NCIT_R145 NCIT_C41879 @default.
- NCIT_C52505 NCIT_R145 NCIT_C42308 @default.
- NCIT_C52505 NCIT_R145 NCIT_C64389 @default.
- NCIT_C52505 NCIT_R37 NCIT_C17133 @default.
- NCIT_C52505 NCIT_R37 NCIT_C17828 @default.
- NCIT_C52505 NCIT_R37 NCIT_C17932 @default.
- NCIT_C52505 NCIT_R37 NCIT_C20480 @default.
- NCIT_C52505 NCIT_R37 NCIT_C20748 @default.
- NCIT_C52505 NCIT_R37 NCIT_C21124 @default.
- NCIT_C52505 NCIT_R37 NCIT_C21128 @default.
- NCIT_C52505 NCIT_R37 NCIT_C21147 @default.
- NCIT_C52505 NCIT_R37 NCIT_C41514 @default.
- NCIT_C52505 NCIT_R40 NCIT_C12219 @default.
- NCIT_C52505 NCIT_R40 NCIT_C13282 @default.
- NCIT_C52505 NCIT_R40 NCIT_C13377 @default.
- NCIT_C52505 NCIT_R40 NCIT_C13432 @default.
- NCIT_C52505 NCIT_R40 NCIT_C13446 @default.
- NCIT_C52505 NCIT_R40 NCIT_C13997 @default.
- NCIT_C52505 NCIT_R40 NCIT_C14135 @default.
- NCIT_C52505 NCIT_R40 NCIT_C32221 @default.
- NCIT_C52505 NCIT_R40 NCIT_C34070 @default.
- NCIT_C52505 NCIT_R41 NCIT_C14182 @default.
- NCIT_C52505 NCIT_R41 NCIT_C14225 @default.
- NCIT_C52505 NCIT_R41 NCIT_C14234 @default.
- NCIT_C52505 NCIT_R41 NCIT_C14250 @default.
- NCIT_C52505 NCIT_R41 NCIT_C14262 @default.
- NCIT_C52505 NCIT_R41 NCIT_C14282 @default.
- NCIT_C52505 NCIT_R41 NCIT_C25796 @default.
- NCIT_C52505 NCIT_R41 NCIT_C79740 @default.
- NCIT_C52505 normalizedInformationContent "100" @default.
- NCIT_C52505 referenceCount "1" @default.
- NCIT_C52505 hasExactSynonym "CAM" @default.
- NCIT_C52505 hasExactSynonym "CCM1" @default.
- NCIT_C52505 hasExactSynonym "Cerebral Cavernous Malformations 1 Gene" @default.
- NCIT_C52505 hasExactSynonym "KRIT1 wt Allele" @default.
- NCIT_C52505 hasExactSynonym "KRIT1, Ankyrin Repeat Containing wt Allele" @default.
- NCIT_C52505 type Class @default.
- NCIT_C52505 isDefinedBy ncit.owl @default.
- NCIT_C52505 label "KRIT1 wt Allele" @default.
- NCIT_C52505 subClassOf NCIT_C16612 @default.
- NCIT_C52505 subClassOf NCIT_C20921 @default.
- NCIT_C52505 subClassOf NCIT_C24267 @default.
- NCIT_C52505 subClassOf NCIT_C52505 @default.
- NCIT_C52505 equivalentClass B286da91aa5fffe9094f46dd8605e7387 @default.
- NCIT_C52505 equivalentClass B712f8346cdc4c7d1e1b97c1885261746 @default.