PMC:5097349 / 11437-11469 JSONTXT

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    AxD_symptoms

    {"project":"AxD_symptoms","denotations":[{"id":"T49","span":{"begin":16,"end":32},"obj":"Phenotype"}],"attributes":[{"id":"A49","pred":"hp_id","subj":"T49","obj":"http://purl.obolibrary.org/obo/HP_0002120"}],"text":"nonspecific WM; cortical atrophy"}