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PMC:5097349 / 5378-6970 JSONTXT

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AxD_symptoms

Id Subject Object Predicate Lexical cue hp_id
T19 606-624 Phenotype denotes cerebellar atrophy http://purl.obolibrary.org/obo/HP_0001272
T20 677-724 Phenotype denotes abnormality in the periventricular white matter http://purl.obolibrary.org/obo/HP_0002518
T21 1419-1437 Phenotype denotes cerebellar atrophy http://purl.obolibrary.org/obo/HP_0001272