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- NCIT_C168800 IAO_0000115 "A genetic variant that is known to have a high likelihood (greater than 90% certainty) to contribute to the development of a disease." @default.
- NCIT_C168800 NCIT_A32 NCIT_C168796 @default.
- NCIT_C168800 NCIT_NHC0 "C168800" @default.
- NCIT_C168800 NCIT_P106 "Nucleotide Sequence" @default.
- NCIT_C168800 NCIT_P108 "Likely Pathogenic Variant" @default.
- NCIT_C168800 NCIT_P208 "CL1379135" @default.
- NCIT_C168800 NCIT_P322 "GDC" @default.
- NCIT_C168800 NCIT_P375 "Likely Pathogenic" @default.
- NCIT_C168800 normalizedInformationContent "100" @default.
- NCIT_C168800 referenceCount "1" @default.
- NCIT_C168800 hasExactSynonym "Likely Pathogenic Variant" @default.
- NCIT_C168800 hasExactSynonym "Likely Pathogenic" @default.
- NCIT_C168800 inSubset NCIT_C157711 @default.
- NCIT_C168800 inSubset NCIT_C177537 @default.
- NCIT_C168800 type Class @default.
- NCIT_C168800 isDefinedBy ncit.owl @default.
- NCIT_C168800 label "Likely Pathogenic Variant" @default.
- NCIT_C168800 subClassOf NCIT_C168800 @default.
- NCIT_C168800 subClassOf NCIT_C17248 @default.
- NCIT_C168800 subClassOf NCIT_C19896 @default.
- NCIT_C168800 subClassOf NCIT_C20181 @default.