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- NCIT_C168802 IAO_0000115 "A genetic variant that is known to not contribute to the development of a disease." @default.
- NCIT_C168802 NCIT_A32 NCIT_C168796 @default.
- NCIT_C168802 NCIT_NHC0 "C168802" @default.
- NCIT_C168802 NCIT_P106 "Nucleotide Sequence" @default.
- NCIT_C168802 NCIT_P108 "Variant Benign" @default.
- NCIT_C168802 NCIT_P208 "CL1378700" @default.
- NCIT_C168802 NCIT_P322 "GDC" @default.
- NCIT_C168802 NCIT_P375 "Benign" @default.
- NCIT_C168802 normalizedInformationContent "100" @default.
- NCIT_C168802 referenceCount "1" @default.
- NCIT_C168802 hasExactSynonym "Benign Variant" @default.
- NCIT_C168802 hasExactSynonym "Benign" @default.
- NCIT_C168802 hasExactSynonym "Variant Benign" @default.
- NCIT_C168802 inSubset NCIT_C157711 @default.
- NCIT_C168802 inSubset NCIT_C177537 @default.
- NCIT_C168802 type Class @default.
- NCIT_C168802 isDefinedBy ncit.owl @default.
- NCIT_C168802 label "Variant Benign" @default.
- NCIT_C168802 subClassOf NCIT_C168802 @default.
- NCIT_C168802 subClassOf NCIT_C17248 @default.
- NCIT_C168802 subClassOf NCIT_C19896 @default.
- NCIT_C168802 subClassOf NCIT_C20181 @default.