PMC:4156421 / 22441-22818 JSONTXT

{"project":"PubTator4TogoVar","denotations":[{"id":"27729","span":{"begin":170,"end":180},"obj":"SNP"}],"attributes":[{"id":"A27729","pred":"resolved_to","subj":"27729","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"}],"text":"We also believe that this is the first whole genome sequence completed on an individual with the MUC5B variant. We are therefore in a position to address, first, whether rs35705950 is merely in LD with other adjacent variants that may actually be disease-causing and, second, whether variants at other loci modulate the risk for fibrotic lung diseases associated with this SNP."}

{"project":"PubTatorOnTogoVar","denotations":[{"id":"27729","span":{"begin":170,"end":180},"obj":"SNP"},{"id":"T1","span":{"begin":170,"end":180},"obj":"SNP"}],"attributes":[{"id":"A27729","pred":"resolved_to","subj":"27729","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs4727443;VariantGroup:6;RS#:4727443"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"},{"id":"A1","pred":"resolved_to","subj":"T1","obj":"tmVar:rs35705950;VariantGroup:27;RS#:35705950"}],"text":"We also believe that this is the first whole genome sequence completed on an individual with the MUC5B variant. We are therefore in a position to address, first, whether rs35705950 is merely in LD with other adjacent variants that may actually be disease-causing and, second, whether variants at other loci modulate the risk for fibrotic lung diseases associated with this SNP."}