PubMed:18470323 / 114-242 JSONTXT

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    LitCoin-sentences

    {"project":"LitCoin-sentences","denotations":[{"id":"T3","span":{"begin":0,"end":128},"obj":"Sentence"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    LitCoin-entities

    {"project":"LitCoin-entities","denotations":[{"id":"5080","span":{"begin":68,"end":100},"obj":"DiseaseOrPhenotypicFeature"},{"id":"5081","span":{"begin":102,"end":106},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A5","pred":"db_id","subj":"5080","obj":"MESH:C537881"},{"id":"A6","pred":"db_id","subj":"5081","obj":"MESH:C537881"}],"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":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    LitCoin_Mondo

    {"project":"LitCoin_Mondo","denotations":[{"id":"T4","span":{"begin":68,"end":100},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":68,"end":93},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":76,"end":93},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0007380"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0004686"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"0018102"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    LitCoin-GeneOrGeneProduct-v2

    {"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T4","span":{"begin":94,"end":100},"obj":"GeneOrGeneProduct"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    LitCoin-GeneOrGeneProduct-v0

    {"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T5","span":{"begin":94,"end":100},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":108,"end":112},"obj":"GeneOrGeneProduct"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    LitCoin-Disease-MeSH

    {"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T2","span":{"begin":76,"end":93},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"originalLabel","subj":"T2","obj":"D003317"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    LitCoin_Mondo_095

    {"project":"LitCoin_Mondo_095","denotations":[{"id":"T2","span":{"begin":68,"end":100},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":102,"end":106},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0007380"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0007380"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    PMID_GLOBAL

    {"project":"PMID_GLOBAL","denotations":[{"id":"T2","span":{"begin":68,"end":100},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":102,"end":106},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0007380"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0007380"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    LitCoin-MeSH-Disease-2

    {"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T2","span":{"begin":76,"end":93},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":102,"end":106},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"ID:","subj":"T2","obj":"D003317"},{"id":"A3","pred":"ID:","subj":"T3","obj":"DISEASE"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    LitCoin-MONDO_bioort2019

    {"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T2","span":{"begin":68,"end":100},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":102,"end":106},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"#label","subj":"T2","obj":"C537881"},{"id":"A3","pred":"#label","subj":"T3","obj":"DISEASE"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    LitCoin-training-merged

    {"project":"LitCoin-training-merged","denotations":[{"id":"T62723","span":{"begin":102,"end":106},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T84989","span":{"begin":68,"end":100},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"#label","subj":"T62723","obj":"DISEASE"},{"id":"A2","pred":"#label","subj":"T84989","obj":"C537881"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T3","span":{"begin":0,"end":128},"obj":"Sentence"},{"id":"T3","span":{"begin":0,"end":128},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    PubCasesHPO

    {"project":"PubCasesHPO","denotations":[{"id":"AB1","span":{"begin":68,"end":93},"obj":"HP:0001149"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}

    PubCasesORDO

    {"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":68,"end":100},"obj":"ORDO:98964"},{"id":"AB2","span":{"begin":102,"end":106},"obj":"ORDO:98964"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"To report the clinical, ophthalmic, and genetic characteristics for lattice corneal dystrophy type I (LCDI) in a Chilean family."}