PubMed:29049388 / 1647-1864 JSONTXT

{"project":"LitCoin-entities-OrganismTaxon-PD","denotations":[{"id":"T8","span":{"begin":43,"end":48},"obj":"OrganismTaxon"},{"id":"T10","span":{"begin":114,"end":119},"obj":"OrganismTaxon"},{"id":"T11","span":{"begin":202,"end":207},"obj":"OrganismTaxon"}],"attributes":[{"id":"A8","pred":"db_id","subj":"T8","obj":"NCBItxid:10090"},{"id":"A9","pred":"db_id","subj":"T8","obj":"NCBItxid:10088"},{"id":"A10","pred":"db_id","subj":"T10","obj":"NCBItxid:9606"},{"id":"A11","pred":"db_id","subj":"T11","obj":"NCBItxid:9606"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin-sentences","denotations":[{"id":"T15","span":{"begin":0,"end":217},"obj":"Sentence"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin-entities","denotations":[{"id":"13494","span":{"begin":29,"end":34},"obj":"SequenceVariant"},{"id":"13495","span":{"begin":35,"end":42},"obj":"GeneOrGeneProduct"},{"id":"13496","span":{"begin":43,"end":48},"obj":"OrganismTaxon"},{"id":"13497","span":{"begin":114,"end":119},"obj":"OrganismTaxon"},{"id":"13498","span":{"begin":120,"end":138},"obj":"DiseaseOrPhenotypicFeature"},{"id":"13499","span":{"begin":202,"end":207},"obj":"OrganismTaxon"}],"attributes":[{"id":"A29","pred":"db_id","subj":"13494","obj":"p|SUB|R|140|Q"},{"id":"A30","pred":"db_id","subj":"13495","obj":"NCBIGene:170484"},{"id":"A31","pred":"db_id","subj":"13496","obj":"NCBITaxon:10090"},{"id":"A32","pred":"db_id","subj":"13497","obj":"NCBITaxon:9606"},{"id":"A33","pred":"db_id","subj":"13498","obj":"MESH:D009404"},{"id":"A34","pred":"db_id","subj":"13499","obj":"NCBITaxon:9606"}],"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":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin_Mondo","denotations":[{"id":"T5","span":{"begin":120,"end":138},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0005377"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin-SeqVar","denotations":[{"id":"T7","span":{"begin":29,"end":34},"obj":"SequenceVariant"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T38","span":{"begin":19,"end":28},"obj":"GeneOrGeneProduct"},{"id":"T39","span":{"begin":35,"end":42},"obj":"GeneOrGeneProduct"},{"id":"T40","span":{"begin":130,"end":138},"obj":"GeneOrGeneProduct"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T22","span":{"begin":19,"end":28},"obj":"GeneOrGeneProduct"},{"id":"T23","span":{"begin":35,"end":42},"obj":"GeneOrGeneProduct"},{"id":"T24","span":{"begin":130,"end":138},"obj":"GeneOrGeneProduct"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T14","span":{"begin":120,"end":138},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T15","span":{"begin":159,"end":166},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A14","pred":"originalLabel","subj":"T14","obj":"D009404"},{"id":"A15","pred":"originalLabel","subj":"T15","obj":"D004194"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T9","span":{"begin":35,"end":42},"obj":"GeneOrGeneProduct"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T12","span":{"begin":120,"end":138},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A12","pred":"mondo_id","subj":"T12","obj":"0005377"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T13","span":{"begin":120,"end":138},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T14","span":{"begin":159,"end":166},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A13","pred":"ID:","subj":"T13","obj":"D009404"},{"id":"A14","pred":"ID:","subj":"T14","obj":"D004194"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T9","span":{"begin":120,"end":138},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A9","pred":"#label","subj":"T9","obj":"D009404"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T5","span":{"begin":43,"end":48},"obj":"OrganismTaxon"},{"id":"T6","span":{"begin":114,"end":119},"obj":"OrganismTaxon"},{"id":"T7","span":{"begin":202,"end":207},"obj":"OrganismTaxon"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T9","span":{"begin":35,"end":42},"obj":"GeneOrGeneProduct"},{"id":"T45427","span":{"begin":120,"end":138},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T23115","span":{"begin":202,"end":207},"obj":"OrganismTaxon"},{"id":"T40596","span":{"begin":114,"end":119},"obj":"OrganismTaxon"},{"id":"T64328","span":{"begin":43,"end":48},"obj":"OrganismTaxon"},{"id":"T74446","span":{"begin":29,"end":34},"obj":"SequenceVariant"}],"attributes":[{"id":"A9","pred":"#label","subj":"T45427","obj":"D009404"}],"text":"In conclusion, the inducible R140Q-podocin mouse model is an auspicious model of the most common genetic cause of human nephrotic syndrome, with a spontaneous disease course strongly reminiscent of the human disorder."}