Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C89802> ?p ?o ?g. }
Showing items 1 to 20 of
20
with 100 items per page.
- NCIT_C89802 IAO_0000115 "A rare sex chromosome abnormality in which a female child has 3 extra X chromosomes." @default.
- NCIT_C89802 NCIT_NHC0 "C89802" @default.
- NCIT_C89802 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C89802 NCIT_P108 "Penta X Syndrome" @default.
- NCIT_C89802 NCIT_P207 "C0265497" @default.
- NCIT_C89802 NCIT_P322 "Cellosaurus" @default.
- NCIT_C89802 normalizedInformationContent "100" @default.
- NCIT_C89802 referenceCount "1" @default.
- NCIT_C89802 hasExactSynonym "49, XXXXX Syndrome" @default.
- NCIT_C89802 hasExactSynonym "Penta X Syndrome" @default.
- NCIT_C89802 hasExactSynonym "XXXXX Syndrome" @default.
- NCIT_C89802 inSubset NCIT_C165258 @default.
- NCIT_C89802 inSubset NCIT_C192842 @default.
- NCIT_C89802 type Class @default.
- NCIT_C89802 isDefinedBy ncit.owl @default.
- NCIT_C89802 label "Penta X Syndrome" @default.
- NCIT_C89802 subClassOf NCIT_C28193 @default.
- NCIT_C89802 subClassOf NCIT_C2991 @default.
- NCIT_C89802 subClassOf NCIT_C7057 @default.
- NCIT_C89802 subClassOf NCIT_C89802 @default.