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- NCIT_C126070 IAO_0000115 "An indication as to whether the condition under study is considered a rare or orphan disease." @default.
- NCIT_C126070 NCIT_NHC0 "C126070" @default.
- NCIT_C126070 NCIT_P106 "Conceptual Entity" @default.
- NCIT_C126070 NCIT_P108 "Rare Disease Indicator" @default.
- NCIT_C126070 NCIT_P208 "CL504668" @default.
- NCIT_C126070 NCIT_P322 "CDISC" @default.
- NCIT_C126070 NCIT_P325 "An indication as to whether the condition under study is considered a rare disease." @default.
- NCIT_C126070 normalizedInformationContent "100" @default.
- NCIT_C126070 referenceCount "1" @default.
- NCIT_C126070 hasExactSynonym "RDIND" @default.
- NCIT_C126070 hasExactSynonym "Rare Disease Indicator" @default.
- NCIT_C126070 inSubset NCIT_C61410 @default.
- NCIT_C126070 inSubset NCIT_C66738 @default.
- NCIT_C126070 inSubset NCIT_C66830 @default.
- NCIT_C126070 inSubset NCIT_C67152 @default.
- NCIT_C126070 type Class @default.
- NCIT_C126070 isDefinedBy ncit.owl @default.
- NCIT_C126070 label "Rare Disease Indicator" @default.
- NCIT_C126070 subClassOf NCIT_C126070 @default.
- NCIT_C126070 subClassOf NCIT_C20181 @default.
- NCIT_C126070 subClassOf NCIT_C25180 @default.