PubMed:10690989 / 0-148 JSONTXT

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"10690989-0#50#55#gene1180","span":{"begin":50,"end":55},"obj":"gene1180"},{"id":"10690989-0#75#93#diseaseC0027127","span":{"begin":75,"end":93},"obj":"diseaseC0027127"},{"id":"10690989-0#75#93#diseaseC2936781","span":{"begin":75,"end":93},"obj":"diseaseC2936781"}],"relations":[{"id":"50#55#gene118075#93#diseaseC0027127","pred":"associated_with","subj":"10690989-0#50#55#gene1180","obj":"10690989-0#75#93#diseaseC0027127"},{"id":"50#55#gene118075#93#diseaseC2936781","pred":"associated_with","subj":"10690989-0#50#55#gene1180","obj":"10690989-0#75#93#diseaseC2936781"}],"text":"Functional consequences of chloride channel gene (CLCN1) mutations causing myotonia congenita.\nOBJECTIVE: To determine the functional consequences o"}