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- NCIT_C34496 NCIT_NHC0 "C34496" @default.
- NCIT_C34496 NCIT_P106 "Finding" @default.
- NCIT_C34496 NCIT_P108 "Defective Color Vision" @default.
- NCIT_C34496 NCIT_P203 "Findings_and_Disorders_Kind" @default.
- NCIT_C34496 NCIT_P310 "Retired_Concept" @default.
- NCIT_C34496 NCIT_P325 "Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the OPSIN genes (on X CHROMOSOME and CHROMOSOME 3, HUMAN) that code the photopigments for red, green and blue." @default.
- NCIT_C34496 NCIT_P98 "See 'Color Blindness'" @default.
- NCIT_C34496 normalizedInformationContent "100" @default.
- NCIT_C34496 referenceCount "1" @default.
- NCIT_C34496 hasExactSynonym "Defective Color Vision" @default.
- NCIT_C34496 type Class @default.
- NCIT_C34496 isDefinedBy ncit.owl @default.
- NCIT_C34496 label "Defective Color Vision" @default.
- NCIT_C34496 subClassOf NCIT_C28428 @default.
- NCIT_C34496 subClassOf NCIT_C34496 @default.
- NCIT_C34496 subClassOf NCIT_C83482 @default.
- NCIT_C34496 deprecated "true" @default.