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- NCIT_C131639 IAO_0000115 "An autosomal dominant disorder characterized by thrombocytopenia, giant platelets, nephritis, and deafness; it is associated with mutation of the MYH9 gene." @default.
- NCIT_C131639 NCIT_NHC0 "C131639" @default.
- NCIT_C131639 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C131639 NCIT_P108 "Epstein Syndrome" @default.
- NCIT_C131639 NCIT_P207 "C0398641" @default.
- NCIT_C131639 NCIT_P322 "NICHD" @default.
- NCIT_C131639 NCIT_P325 "An autosomal dominant disorder characterized by thrombocytopenia, giant platelets, nephritis, and deafness; it is associated with mutation of the MYH9 gene." @default.
- NCIT_C131639 NCIT_R176 NCIT_C16612 @default.
- NCIT_C131639 NCIT_R176 NCIT_C20744 @default.
- NCIT_C131639 NCIT_R176 NCIT_C20745 @default.
- NCIT_C131639 NCIT_R176 NCIT_C97646 @default.
- NCIT_C131639 normalizedInformationContent "100" @default.
- NCIT_C131639 referenceCount "1" @default.
- NCIT_C131639 hasExactSynonym "Epstein Syndrome" @default.
- NCIT_C131639 inSubset NCIT_C132009 @default.
- NCIT_C131639 inSubset NCIT_C90259 @default.
- NCIT_C131639 type Class @default.
- NCIT_C131639 isDefinedBy ncit.owl @default.
- NCIT_C131639 label "Epstein Syndrome" @default.
- NCIT_C131639 subClassOf B87d7614b722d9aa516f19700cb1e897d @default.
- NCIT_C131639 subClassOf B9e038e615caefca3cde1796cb6264a09 @default.
- NCIT_C131639 subClassOf NCIT_C131639 @default.
- NCIT_C131639 subClassOf NCIT_C158788 @default.
- NCIT_C131639 subClassOf NCIT_C28193 @default.
- NCIT_C131639 subClassOf NCIT_C2991 @default.
- NCIT_C131639 subClassOf NCIT_C4873 @default.
- NCIT_C131639 subClassOf NCIT_C53529 @default.
- NCIT_C131639 subClassOf NCIT_C53543 @default.
- NCIT_C131639 subClassOf NCIT_C53547 @default.
- NCIT_C131639 subClassOf NCIT_C7057 @default.