PubMed:18681856 / 0-144 JSONTXT

{"project":"LitCoin-sentences","denotations":[{"id":"T1","span":{"begin":0,"end":144},"obj":"Sentence"}],"text":"Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene."}

{"project":"LitCoin-entities","denotations":[{"id":"5436","span":{"begin":31,"end":61},"obj":"DiseaseOrPhenotypicFeature"},{"id":"5437","span":{"begin":102,"end":109},"obj":"SequenceVariant"},{"id":"5438","span":{"begin":118,"end":138},"obj":"GeneOrGeneProduct"}],"attributes":[{"id":"A1","pred":"db_id","subj":"5436","obj":"MESH:C563786"},{"id":"A2","pred":"db_id","subj":"5437","obj":"DBSNP:rs121908864"},{"id":"A3","pred":"db_id","subj":"5438","obj":"NCBIGene:7253"}],"namespaces":[{"prefix":"_base","uri":"https://w3id.org/biolink/vocab/"},{"prefix":"MESH","uri":"http://id.nlm.nih.gov/mesh/"},{"prefix":"NCBITaxon","uri":"https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id="},{"prefix":"NCBIGene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"OMIM","uri":"https://www.omim.org/entry/"},{"prefix":"DBSNP","uri":"https://www.ncbi.nlm.nih.gov/snp/"}],"text":"Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene."}

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{"project":"LitCoin-SeqVar","denotations":[{"id":"T1","span":{"begin":102,"end":109},"obj":"SequenceVariant"}],"text":"Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":118,"end":138},"obj":"GeneOrGeneProduct"}],"text":"Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene."}

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{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":31,"end":61},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"originalLabel","subj":"T1","obj":"C563786"}],"text":"Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene."}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":118,"end":138},"obj":"GeneOrGeneProduct"}],"text":"Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":31,"end":61},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0012203"}],"text":"Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":31,"end":61},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"C563786"}],"text":"Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":31,"end":61},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"C563786"}],"text":"Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T74312","span":{"begin":118,"end":138},"obj":"GeneOrGeneProduct"},{"id":"T2566","span":{"begin":31,"end":61},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T50756","span":{"begin":102,"end":109},"obj":"SequenceVariant"}],"attributes":[{"id":"A45571","pred":"#label","subj":"T2566","obj":"C563786"}],"text":"Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":144},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":144},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene."}

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