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- NCIT_C181345 IAO_0000115 "A categorization of the phenotypic consequence of the genetic variation." @default.
- NCIT_C181345 NCIT_NHC0 "C181345" @default.
- NCIT_C181345 NCIT_P106 "Intellectual Product" @default.
- NCIT_C181345 NCIT_P108 "Genetic Variation Functional Impact Classification" @default.
- NCIT_C181345 NCIT_P208 "CL1664564" @default.
- NCIT_C181345 NCIT_P322 "CDISC" @default.
- NCIT_C181345 NCIT_P325 "A categorization of the phenotypic or clinical significance of the genomic variation." @default.
- NCIT_C181345 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C181345 referenceCount "2" @default.
- NCIT_C181345 hasExactSynonym "Genetic Variation Functional Impact Classification" @default.
- NCIT_C181345 hasExactSynonym "VARIANT IMPACT CLASSIFICATION" @default.
- NCIT_C181345 inSubset NCIT_C181180 @default.
- NCIT_C181345 inSubset NCIT_C61410 @default.
- NCIT_C181345 inSubset NCIT_C66830 @default.
- NCIT_C181345 type Class @default.
- NCIT_C181345 isDefinedBy ncit.owl @default.
- NCIT_C181345 label "Genetic Variation Functional Impact Classification" @default.
- NCIT_C181345 subClassOf NCIT_C181345 @default.
- NCIT_C181345 subClassOf NCIT_C20181 @default.
- NCIT_C181345 subClassOf NCIT_C25161 @default.
- NCIT_C181345 subClassOf NCIT_C97331 @default.