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- NCIT_C36630 IAO_0000115 "A chromosomal abnormality consisting of the presence of one copy of the X chromosome and the complete absence of a second sex chromosome (X or Y) in somatic cells." @default.
- NCIT_C36630 NCIT_NHC0 "C36630" @default.
- NCIT_C36630 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C36630 NCIT_P108 "Monosomy X" @default.
- NCIT_C36630 NCIT_P208 "CL550569" @default.
- NCIT_C36630 NCIT_P366 "Monosomy_X" @default.
- NCIT_C36630 NCIT_R173 NCIT_C12219 @default.
- NCIT_C36630 NCIT_R173 NCIT_C13202 @default.
- NCIT_C36630 NCIT_R173 NCIT_C13203 @default.
- NCIT_C36630 NCIT_R173 NCIT_C13285 @default.
- NCIT_C36630 NCIT_R173 NCIT_C13404 @default.
- NCIT_C36630 NCIT_R173 NCIT_C14134 @default.
- NCIT_C36630 NCIT_R173 NCIT_C21599 @default.
- NCIT_C36630 normalizedInformationContent "92.730304365937428" @default.
- NCIT_C36630 referenceCount "3" @default.
- NCIT_C36630 hasExactSynonym "Monosomy X" @default.
- NCIT_C36630 type Class @default.
- NCIT_C36630 isDefinedBy ncit.owl @default.
- NCIT_C36630 label "Monosomy X" @default.
- NCIT_C36630 subClassOf Baebb993bb65c57a0e52b38fb8f845a49 @default.
- NCIT_C36630 subClassOf Bcd92ad34094297f24045f28030b70e81 @default.
- NCIT_C36630 subClassOf NCIT_C2873 @default.
- NCIT_C36630 subClassOf NCIT_C2950 @default.
- NCIT_C36630 subClassOf NCIT_C3239 @default.
- NCIT_C36630 subClassOf NCIT_C36630 @default.
- NCIT_C36630 subClassOf NCIT_C3910 @default.
- NCIT_C36630 subClassOf NCIT_C6825 @default.