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- NCIT_C131620 IAO_0000115 "A mutation that appears in the genome of the germ cells and is associated with increased risk of disease." @default.
- NCIT_C131620 NCIT_NHC0 "C131620" @default.
- NCIT_C131620 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C131620 NCIT_P107 "Deleterious Germline Mutation" @default.
- NCIT_C131620 NCIT_P108 "Deleterious Germline Mutation" @default.
- NCIT_C131620 NCIT_P208 "CL514628" @default.
- NCIT_C131620 NCIT_P322 "CTRP" @default.
- NCIT_C131620 normalizedInformationContent "100" @default.
- NCIT_C131620 referenceCount "1" @default.
- NCIT_C131620 hasExactSynonym "Deleterious Germline Mutation" @default.
- NCIT_C131620 inSubset NCIT_C116977 @default.
- NCIT_C131620 inSubset NCIT_C142799 @default.
- NCIT_C131620 inSubset NCIT_C142800 @default.
- NCIT_C131620 type Class @default.
- NCIT_C131620 isDefinedBy ncit.owl @default.
- NCIT_C131620 label "Deleterious Germline Mutation" @default.
- NCIT_C131620 subClassOf NCIT_C131620 @default.
- NCIT_C131620 subClassOf NCIT_C17666 @default.
- NCIT_C131620 subClassOf NCIT_C36391 @default.
- NCIT_C131620 subClassOf NCIT_C3910 @default.
- NCIT_C131620 subClassOf NCIT_C45576 @default.
- NCIT_C131620 subClassOf NCIT_C93102 @default.
- NCIT_C131620 subClassOf NCIT_C97926 @default.