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- NCIT_C178390 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the SAMD9L gene, encoding sterile alpha motif domain-containing protein 9-like. It is characterized by an increased risk of developing myelodysplastic syndrome." @default.
- NCIT_C178390 NCIT_A13 NCIT_C168734 @default.
- NCIT_C178390 NCIT_NHC0 "C178390" @default.
- NCIT_C178390 NCIT_P106 "Finding" @default.
- NCIT_C178390 NCIT_P108 "SAMD9L-Related Predisposition to Myelodysplastic Syndrome" @default.
- NCIT_C178390 NCIT_P208 "CL1647850" @default.
- NCIT_C178390 NCIT_P322 "CCPS" @default.
- NCIT_C178390 normalizedInformationContent "100" @default.
- NCIT_C178390 referenceCount "1" @default.
- NCIT_C178390 hasExactSynonym "SAMD9L-Related Myelodysplastic Syndrome Predisposition" @default.
- NCIT_C178390 hasExactSynonym "SAMD9L-Related Predisposition to Myelodysplastic Syndrome" @default.
- NCIT_C178390 inSubset NCIT_C177281 @default.
- NCIT_C178390 inSubset NCIT_C177516 @default.
- NCIT_C178390 type Class @default.
- NCIT_C178390 isDefinedBy ncit.owl @default.
- NCIT_C178390 label "SAMD9L-Related Predisposition to Myelodysplastic Syndrome" @default.
- NCIT_C178390 subClassOf NCIT_C178384 @default.
- NCIT_C178390 subClassOf NCIT_C178390 @default.
- NCIT_C178390 subClassOf NCIT_C3367 @default.
- NCIT_C178390 subClassOf NCIT_C36278 @default.
- NCIT_C178390 subClassOf NCIT_C36289 @default.
- NCIT_C178390 subClassOf NCIT_C7057 @default.