PMC:5097349 / 11377-11481 JSONTXT

{"project":"AxD_symptoms","denotations":[{"id":"T46","span":{"begin":14,"end":25},"obj":"Phenotype"},{"id":"T47","span":{"begin":27,"end":35},"obj":"Phenotype"},{"id":"T48","span":{"begin":37,"end":59},"obj":"Phenotype"},{"id":"T49","span":{"begin":76,"end":92},"obj":"Phenotype"}],"attributes":[{"id":"A46","pred":"hp_id","subj":"T46","obj":"http://purl.obolibrary.org/obo/HP_0002354"},{"id":"A47","pred":"hp_id","subj":"T47","obj":"http://purl.obolibrary.org/obo/HP_0000726"},{"id":"A48","pred":"hp_id","subj":"T48","obj":"http://purl.obolibrary.org/obo/HP_0000924"},{"id":"A49","pred":"hp_id","subj":"T49","obj":"http://purl.obolibrary.org/obo/HP_0002120"}],"text":"NHD/PLOSL PP, memory loss, dementia, skeletal abnormalities nonspecific WM; cortical atrophy TREM2 DAP12"}