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- NCIT_C136636 IAO_0000115 "A point mutation in a gene that is a member of the RAS gene family that encodes an amino acid substitution in a RAS family protein." @default.
- NCIT_C136636 NCIT_A13 NCIT_C17060 @default.
- NCIT_C136636 NCIT_A13 NCIT_C25785 @default.
- NCIT_C136636 NCIT_A13 NCIT_C25786 @default.
- NCIT_C136636 NCIT_NHC0 "C136636" @default.
- NCIT_C136636 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C136636 NCIT_P107 "Non-synonymous RAS Family Gene Mutation" @default.
- NCIT_C136636 NCIT_P108 "Non-synonymous RAS Family Gene Mutation" @default.
- NCIT_C136636 NCIT_P208 "CL524480" @default.
- NCIT_C136636 NCIT_P322 "CTRP" @default.
- NCIT_C136636 normalizedInformationContent "72.907058208479896" @default.
- NCIT_C136636 referenceCount "60" @default.
- NCIT_C136636 hasExactSynonym "Non-synonymous RAS Family Gene Mutation" @default.
- NCIT_C136636 hasExactSynonym "RAS Family Gene Missense Mutation" @default.
- NCIT_C136636 inSubset NCIT_C116977 @default.
- NCIT_C136636 inSubset NCIT_C142799 @default.
- NCIT_C136636 inSubset NCIT_C142800 @default.
- NCIT_C136636 type Class @default.
- NCIT_C136636 isDefinedBy ncit.owl @default.
- NCIT_C136636 label "Non-synonymous RAS Family Gene Mutation" @default.
- NCIT_C136636 subClassOf NCIT_C132229 @default.
- NCIT_C136636 subClassOf NCIT_C136636 @default.
- NCIT_C136636 subClassOf NCIT_C18133 @default.
- NCIT_C136636 subClassOf NCIT_C36327 @default.
- NCIT_C136636 subClassOf NCIT_C36391 @default.
- NCIT_C136636 subClassOf NCIT_C3910 @default.
- NCIT_C136636 subClassOf NCIT_C45576 @default.
- NCIT_C136636 subClassOf NCIT_C62200 @default.
- NCIT_C136636 subClassOf NCIT_C97926 @default.