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- B142f6decddc69d3bd9cf11a4f558e5a7 hasDbXref "Orphanet:363746" @default.
- B142f6decddc69d3bd9cf11a4f558e5a7 hasDbXref "https://github.com/obophenotype/human-phenotype-ontology/issues/3570" @default.
- B142f6decddc69d3bd9cf11a4f558e5a7 type Axiom @default.
- B142f6decddc69d3bd9cf11a4f558e5a7 annotatedProperty IAO_0000115 @default.
- B142f6decddc69d3bd9cf11a4f558e5a7 annotatedSource MONDO_0018211 @default.
- B142f6decddc69d3bd9cf11a4f558e5a7 annotatedTarget "Balint syndrome is a rare neurologic disease characterized by the triad of optic ataxia, ocular apraxia and simultanagnosia due to posterior parietal lobe lesions. Patients report ophthalmologic difficulties in the absence of underlying ophthalomologic anomalies and present severe visual and spatial disabilities in locating and reaching objects, initiating voluntary eye movements and perceiving more than one object at a time." @default.