PubMed:27930654 / 279-507 JSONTXT

{"project":"LitCoin-entities","denotations":[{"id":"11796","span":{"begin":34,"end":59},"obj":"DiseaseOrPhenotypicFeature"},{"id":"11797","span":{"begin":61,"end":73},"obj":"DiseaseOrPhenotypicFeature"},{"id":"11798","span":{"begin":83,"end":103},"obj":"DiseaseOrPhenotypicFeature"},{"id":"11799","span":{"begin":108,"end":129},"obj":"DiseaseOrPhenotypicFeature"},{"id":"11800","span":{"begin":131,"end":134},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"db_id","subj":"11796","obj":"MESH:D030342"},{"id":"A5","pred":"db_id","subj":"11797","obj":"MESH:D000072661"},{"id":"A6","pred":"db_id","subj":"11798","obj":"MESH:D012174"},{"id":"A7","pred":"db_id","subj":"11799","obj":"MESH:D020788"},{"id":"A8","pred":"db_id","subj":"11800","obj":"MESH:D020788"}],"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":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}

{"project":"LitCoin-sentences","denotations":[{"id":"T3","span":{"begin":0,"end":228},"obj":"Sentence"}],"text":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}

{"project":"LitCoin-entities-OrganismTaxon-PD","denotations":[{"id":"T1","span":{"begin":44,"end":49},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"NCBItxid:9606"}],"text":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}

{"project":"LitCoin_Mondo","denotations":[{"id":"T1","span":{"begin":34,"end":43},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":61,"end":73},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":83,"end":103},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":83,"end":92},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":108,"end":129},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0021152"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0005308"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0019200"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0002708"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0015229"}],"text":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T9","span":{"begin":0,"end":7},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":83,"end":92},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":121,"end":129},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":158,"end":162},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":195,"end":204},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":212,"end":220},"obj":"GeneOrGeneProduct"}],"text":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T7","span":{"begin":121,"end":129},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":212,"end":220},"obj":"GeneOrGeneProduct"}],"text":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}

{"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T1","span":{"begin":44,"end":49},"obj":"OrganismTaxon"}],"text":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":61,"end":73},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":83,"end":103},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":108,"end":129},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":131,"end":134},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"originalLabel","subj":"T1","obj":"D000072661"},{"id":"A2","pred":"originalLabel","subj":"T2","obj":"D012174"},{"id":"A3","pred":"originalLabel","subj":"T3","obj":"D020788"},{"id":"A4","pred":"originalLabel","subj":"T4","obj":"D020788"}],"text":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":61,"end":73},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":83,"end":103},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":108,"end":129},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":131,"end":134},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0005308"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0019200"},{"id":"A3","pred":"mondo_id","subj":"T2","obj":"0008377"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0015229"},{"id":"A5","pred":"mondo_id","subj":"T4","obj":"0014432"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"0015229"},{"id":"A7","pred":"mondo_id","subj":"T6","obj":"0014432"}],"text":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":34,"end":59},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":61,"end":73},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":83,"end":103},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":108,"end":129},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":131,"end":134},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"DISEASE"},{"id":"A2","pred":"ID:","subj":"T2","obj":"D000072661"},{"id":"A3","pred":"ID:","subj":"T3","obj":"D012174"},{"id":"A4","pred":"ID:","subj":"T4","obj":"D020788"},{"id":"A5","pred":"ID:","subj":"T5","obj":"D020788"}],"text":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":34,"end":59},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":61,"end":73},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":83,"end":103},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":108,"end":129},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":131,"end":134},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"DISEASE"},{"id":"A2","pred":"#label","subj":"T2","obj":"D000072661"},{"id":"A3","pred":"#label","subj":"T3","obj":"D012174"},{"id":"A4","pred":"#label","subj":"T4","obj":"D020788"},{"id":"A5","pred":"#label","subj":"T5","obj":"D020788"}],"text":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T15507","span":{"begin":131,"end":134},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T56269","span":{"begin":108,"end":129},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T57409","span":{"begin":83,"end":103},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T71830","span":{"begin":61,"end":73},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T68457","span":{"begin":34,"end":59},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T45910","span":{"begin":44,"end":49},"obj":"OrganismTaxon"}],"attributes":[{"id":"A47926","pred":"#label","subj":"T15507","obj":"D020788"},{"id":"A53280","pred":"#label","subj":"T56269","obj":"D020788"},{"id":"A65386","pred":"#label","subj":"T57409","obj":"D012174"},{"id":"A51807","pred":"#label","subj":"T71830","obj":"D000072661"},{"id":"A16455","pred":"#label","subj":"T68457","obj":"DISEASE"}],"text":"Defects in these organelles cause inherited human disorders (ciliopathies) such as retinitis pigmentosa and Bardet-Biedl syndrome (BBS), frequently affecting many physiological and developmental processes across multiple organs."}