PubMed:29049388 / 0-224 JSONTXT

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    LitCoin-entities-OrganismTaxon-PD

    {"project":"LitCoin-entities-OrganismTaxon-PD","denotations":[{"id":"T1","span":{"begin":13,"end":18},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"NCBItxid:10090"},{"id":"A2","pred":"db_id","subj":"T1","obj":"NCBItxid:10088"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin-sentences

    {"project":"LitCoin-sentences","denotations":[{"id":"T1","span":{"begin":0,"end":72},"obj":"Sentence"},{"id":"T2","span":{"begin":73,"end":156},"obj":"Sentence"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin-entities

    {"project":"LitCoin-entities","denotations":[{"id":"13466","span":{"begin":13,"end":18},"obj":"OrganismTaxon"},{"id":"13467","span":{"begin":28,"end":35},"obj":"GeneOrGeneProduct"},{"id":"13468","span":{"begin":53,"end":71},"obj":"DiseaseOrPhenotypicFeature"},{"id":"13469","span":{"begin":90,"end":95},"obj":"GeneOrGeneProduct"},{"id":"13470","span":{"begin":111,"end":118},"obj":"GeneOrGeneProduct"},{"id":"13471","span":{"begin":137,"end":155},"obj":"DiseaseOrPhenotypicFeature"},{"id":"13472","span":{"begin":173,"end":180},"obj":"GeneOrGeneProduct"},{"id":"13473","span":{"begin":191,"end":196},"obj":"SequenceVariant"}],"attributes":[{"id":"A1","pred":"db_id","subj":"13466","obj":"NCBITaxon:10090"},{"id":"A2","pred":"db_id","subj":"13467","obj":"NCBIGene:170484"},{"id":"A3","pred":"db_id","subj":"13468","obj":"MESH:D009404"},{"id":"A4","pred":"db_id","subj":"13469","obj":"NCBIGene:7827"},{"id":"A5","pred":"db_id","subj":"13470","obj":"NCBIGene:7827"},{"id":"A6","pred":"db_id","subj":"13471","obj":"MESH:D009404"},{"id":"A7","pred":"db_id","subj":"13472","obj":"NCBIGene:7827"},{"id":"A8","pred":"db_id","subj":"13473","obj":"DBSNP:rs74315342"}],"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":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin_Mondo

    {"project":"LitCoin_Mondo","denotations":[{"id":"T1","span":{"begin":53,"end":71},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":137,"end":155},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0005377"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0005377"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin-SeqVar

    {"project":"LitCoin-SeqVar","denotations":[{"id":"T1","span":{"begin":191,"end":196},"obj":"SequenceVariant"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin-GeneOrGeneProduct-v0

    {"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T1","span":{"begin":3,"end":12},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":28,"end":35},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":36,"end":44},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":63,"end":71},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":73,"end":82},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":90,"end":95},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":111,"end":118},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":147,"end":155},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":173,"end":180},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":181,"end":189},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":217,"end":222},"obj":"GeneOrGeneProduct"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin-GeneOrGeneProduct-v2

    {"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":3,"end":12},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":28,"end":35},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":63,"end":71},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":90,"end":95},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":111,"end":118},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":147,"end":155},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":173,"end":180},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":217,"end":222},"obj":"GeneOrGeneProduct"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin-Disease-MeSH

    {"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":53,"end":71},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":137,"end":155},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"originalLabel","subj":"T1","obj":"D009404"},{"id":"A2","pred":"originalLabel","subj":"T2","obj":"D009404"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin-GeneOrGeneProduct-v3

    {"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":28,"end":35},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":90,"end":95},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":111,"end":118},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":173,"end":180},"obj":"GeneOrGeneProduct"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin_Mondo_095

    {"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":53,"end":71},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":90,"end":95},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":126,"end":155},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0005377"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0044765"},{"id":"A3","pred":"mondo_id","subj":"T2","obj":"0010974"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0002350"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin-MeSH-Disease-2

    {"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":53,"end":71},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":137,"end":155},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D009404"},{"id":"A2","pred":"ID:","subj":"T2","obj":"D009404"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin-MONDO_bioort2019

    {"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":53,"end":71},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":137,"end":155},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"D009404"},{"id":"A2","pred":"#label","subj":"T2","obj":"D009404"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin-NCBITaxon-2

    {"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T1","span":{"begin":13,"end":18},"obj":"OrganismTaxon"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}

    LitCoin-training-merged

    {"project":"LitCoin-training-merged","denotations":[{"id":"T4","span":{"begin":173,"end":180},"obj":"GeneOrGeneProduct"},{"id":"T10911","span":{"begin":111,"end":118},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":90,"end":95},"obj":"GeneOrGeneProduct"},{"id":"T12364","span":{"begin":28,"end":35},"obj":"GeneOrGeneProduct"},{"id":"T41330","span":{"begin":137,"end":155},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T24073","span":{"begin":53,"end":71},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T15197","span":{"begin":13,"end":18},"obj":"OrganismTaxon"},{"id":"T66323","span":{"begin":191,"end":196},"obj":"SequenceVariant"}],"attributes":[{"id":"A16216","pred":"#label","subj":"T41330","obj":"D009404"},{"id":"A95318","pred":"#label","subj":"T24073","obj":"D009404"}],"text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early d"}