PubMed:26900322 / 1240-1532 JSONTXT

{"project":"LitCoin-entities","denotations":[{"id":"11084","span":{"begin":104,"end":107},"obj":"GeneOrGeneProduct"},{"id":"11085","span":{"begin":108,"end":117},"obj":"SequenceVariant"},{"id":"11086","span":{"begin":121,"end":129},"obj":"OrganismTaxon"},{"id":"11087","span":{"begin":135,"end":147},"obj":"DiseaseOrPhenotypicFeature"},{"id":"11088","span":{"begin":165,"end":173},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A23","pred":"db_id","subj":"11084","obj":"NCBIGene:3426"},{"id":"A24","pred":"db_id","subj":"11085","obj":"DBSNP:rs7356506"},{"id":"A25","pred":"db_id","subj":"11086","obj":"NCBITaxon:9606"},{"id":"A26","pred":"db_id","subj":"11087","obj":"MESH:D014607"},{"id":"A27","pred":"db_id","subj":"11088","obj":"MESH:D002386"}],"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":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin-sentences","denotations":[{"id":"T14","span":{"begin":0,"end":292},"obj":"Sentence"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin_Mondo","denotations":[{"id":"T3","span":{"begin":165,"end":173},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0005129"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin-SeqVar","denotations":[{"id":"T5","span":{"begin":108,"end":117},"obj":"SequenceVariant"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T16","span":{"begin":53,"end":64},"obj":"GeneOrGeneProduct"},{"id":"T17","span":{"begin":139,"end":147},"obj":"GeneOrGeneProduct"},{"id":"T18","span":{"begin":165,"end":173},"obj":"GeneOrGeneProduct"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T9","span":{"begin":139,"end":147},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":165,"end":173},"obj":"GeneOrGeneProduct"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T10","span":{"begin":135,"end":147},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":165,"end":173},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A10","pred":"originalLabel","subj":"T10","obj":"D014607"},{"id":"A11","pred":"originalLabel","subj":"T11","obj":"D002386"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T8","span":{"begin":104,"end":107},"obj":"GeneOrGeneProduct"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T10","span":{"begin":135,"end":147},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":165,"end":173},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A10","pred":"mondo_id","subj":"T10","obj":"0018092"},{"id":"A11","pred":"mondo_id","subj":"T11","obj":"0005129"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T8","span":{"begin":135,"end":147},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":165,"end":173},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"ID:","subj":"T8","obj":"D014607"},{"id":"A9","pred":"ID:","subj":"T9","obj":"D002386"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T8","span":{"begin":135,"end":147},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":165,"end":173},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"#label","subj":"T8","obj":"D014607"},{"id":"A9","pred":"#label","subj":"T9","obj":"D002386"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T4","span":{"begin":121,"end":129},"obj":"OrganismTaxon"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin-Chemical-MeSH-CHEBI","denotations":[{"id":"T9","span":{"begin":104,"end":107},"obj":"ChemicalEntity"}],"attributes":[{"id":"A9","pred":"ID:","subj":"T9","obj":"C010073"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T9","span":{"begin":104,"end":107},"obj":"ChemicalEntity"},{"id":"T60582","span":{"begin":104,"end":107},"obj":"GeneOrGeneProduct"},{"id":"T50868","span":{"begin":165,"end":173},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12807","span":{"begin":135,"end":147},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T57425","span":{"begin":121,"end":129},"obj":"OrganismTaxon"},{"id":"T1460","span":{"begin":108,"end":117},"obj":"SequenceVariant"}],"attributes":[{"id":"A9","pred":"ID:","subj":"T9","obj":"C010073"},{"id":"A66520","pred":"#label","subj":"T50868","obj":"D002386"},{"id":"A20394","pred":"#label","subj":"T12807","obj":"D014607"}],"text":"Furthermore, there were significant decreases in the frequencies of the G allele and GG homozygosity in CFI-rs7356506 in patients with VKH syndrome with complicated cataract compared to the controls (p\u003c0.001, OR=0.357, 95% CI=0.197-0.648; p\u003c0.001, OR=0.273, 95% CI=0.135-0.551, respectively)."}