PubMed:18470323 / 0-143 JSONTXT

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{"project":"PubTator4TogoVar","denotations":[{"id":"18470323_0","span":{"begin":63,"end":68},"obj":"ProteinMutation"}],"attributes":[{"id":"18470323_0_ProteinMutation","pred":"proteinmutation","subj":"18470323_0","obj":"rs121909210"}],"text":"Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.\nPURPOSE: To report the clinical, ophth"}

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{"project":"LitCoin_Mondo","denotations":[{"id":"T1","span":{"begin":25,"end":57},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":25,"end":50},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":33,"end":50},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0007380"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0004686"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0018102"}],"text":"Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.\nPURPOSE: To report the clinical, ophth"}

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{"project":"PMID_GLOBAL","denotations":[{"id":"T1","span":{"begin":25,"end":57},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0007380"}],"text":"Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.\nPURPOSE: To report the clinical, ophth"}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":33,"end":50},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D003317"}],"text":"Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.\nPURPOSE: To report the clinical, ophth"}

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{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":104},"obj":"Sentence"},{"id":"TextSentencer_T2","span":{"begin":105,"end":113},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":104},"obj":"Sentence"},{"id":"T2","span":{"begin":105,"end":113},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.\nPURPOSE: To report the clinical, ophth"}

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{"project":"DisGeNET5_variant_disease","denotations":[{"id":"18470323-0#63#68#geners121909210","span":{"begin":63,"end":68},"obj":"geners121909210"},{"id":"18470323-0#25#57#diseaseC1690006","span":{"begin":25,"end":57},"obj":"diseaseC1690006"}],"relations":[{"id":"63#68#geners12190921025#57#diseaseC1690006","pred":"associated_with","subj":"18470323-0#63#68#geners121909210","obj":"18470323-0#25#57#diseaseC1690006"}],"text":"Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.\nPURPOSE: To report the clinical, ophth"}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"18470323-0#85#90#gene7045","span":{"begin":85,"end":90},"obj":"gene7045"},{"id":"18470323-0#92#97#gene7045","span":{"begin":92,"end":97},"obj":"gene7045"},{"id":"18470323-0#25#57#diseaseC1690006","span":{"begin":25,"end":57},"obj":"diseaseC1690006"}],"relations":[{"id":"85#90#gene704525#57#diseaseC1690006","pred":"associated_with","subj":"18470323-0#85#90#gene7045","obj":"18470323-0#25#57#diseaseC1690006"},{"id":"92#97#gene704525#57#diseaseC1690006","pred":"associated_with","subj":"18470323-0#92#97#gene7045","obj":"18470323-0#25#57#diseaseC1690006"}],"text":"Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.\nPURPOSE: To report the clinical, ophth"}

{"project":"PubCasesHPO","denotations":[{"id":"TI1","span":{"begin":25,"end":50},"obj":"HP:0001149"}],"text":"Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.\nPURPOSE: To report the clinical, ophth"}

{"project":"PubCasesORDO","denotations":[{"id":"TI1","span":{"begin":25,"end":57},"obj":"ORDO:98964"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.\nPURPOSE: To report the clinical, ophth"}

{"project":"tmVarCorpus","denotations":[{"id":"T1","span":{"begin":63,"end":68},"obj":"ProteinMutation:p|SUB|R|124|C"}],"text":"Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.\nPURPOSE: To report the clinical, ophth"}