Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C74988> ?p ?o ?g. }
Showing items 1 to 29 of
29
with 100 items per page.
- NCIT_C74988 IAO_0000115 "A rare disorder characterized by the failure of the forebrain to divide into distinct hemispheres. It is associated with craniofacial abnormalities, developmental abnormalities, and seizures." @default.
- NCIT_C74988 NCIT_NHC0 "C74988" @default.
- NCIT_C74988 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C74988 NCIT_P108 "Holoprosencephaly" @default.
- NCIT_C74988 NCIT_P207 "C4011586" @default.
- NCIT_C74988 NCIT_P322 "Cellosaurus" @default.
- NCIT_C74988 NCIT_P322 "NICHD" @default.
- NCIT_C74988 NCIT_P325 "Incomplete development of the forebrain that may be associated with midfacial anomalies and pituitary hormone deficiencies." @default.
- NCIT_C74988 NCIT_P366 "Holoprosencephaly" @default.
- NCIT_C74988 normalizedInformationContent "84.76342111748103" @default.
- NCIT_C74988 referenceCount "10" @default.
- NCIT_C74988 hasExactSynonym "Holoprosencephaly Sequence" @default.
- NCIT_C74988 hasExactSynonym "Holoprosencephaly" @default.
- NCIT_C74988 inSubset NCIT_C118467 @default.
- NCIT_C74988 inSubset NCIT_C165258 @default.
- NCIT_C74988 inSubset NCIT_C192842 @default.
- NCIT_C74988 inSubset NCIT_C90259 @default.
- NCIT_C74988 inSubset NCIT_C99147 @default.
- NCIT_C74988 type Class @default.
- NCIT_C74988 isDefinedBy ncit.owl @default.
- NCIT_C74988 label "Holoprosencephaly" @default.
- NCIT_C74988 subClassOf NCIT_C28193 @default.
- NCIT_C74988 subClassOf NCIT_C2991 @default.
- NCIT_C74988 subClassOf NCIT_C4873 @default.
- NCIT_C74988 subClassOf NCIT_C53529 @default.
- NCIT_C74988 subClassOf NCIT_C53543 @default.
- NCIT_C74988 subClassOf NCIT_C53547 @default.
- NCIT_C74988 subClassOf NCIT_C7057 @default.
- NCIT_C74988 subClassOf NCIT_C74988 @default.