PubMed:20052765 / 293-455 JSONTXT

{"project":"PubMed_ArguminSci","denotations":[{"id":"T3","span":{"begin":0,"end":162},"obj":"DRI_Challenge"}],"text":"Mutations in the CLN5 gene result in the Finnish variant late infantile NCL characterized by gradual loss of vision, epileptic seizures, and mental deterioration."}

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":101,"end":115},"obj":"HP_0000572"},{"id":"T2","span":{"begin":127,"end":135},"obj":"HP_0001250"},{"id":"T3","span":{"begin":141,"end":161},"obj":"HP_0001268"}],"text":"Mutations in the CLN5 gene result in the Finnish variant late infantile NCL characterized by gradual loss of vision, epileptic seizures, and mental deterioration."}