PubMed:15000256 / 0-165 JSONTXT

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{"project":"DisGeNET5_gene_disease","denotations":[{"id":"15000256-0#56#60#gene2332","span":{"begin":56,"end":60},"obj":"gene2332"},{"id":"15000256-0#69#77#diseaseC0004352","span":{"begin":69,"end":77},"obj":"diseaseC0004352"}],"relations":[{"id":"56#60#gene233269#77#diseaseC0004352","pred":"associated_with","subj":"15000256-0#56#60#gene2332","obj":"15000256-0#69#77#diseaseC0004352"}],"text":"Single-strand conformation polymorphism analysis of the FMR1 gene in autistic and mentally retarded children in Japan.\nFragile X syndrome is one of the most common c"}