PubMed:21903317 / 0-108
Annnotations
LitCoin-sentences
{"project":"LitCoin-sentences","denotations":[{"id":"T1","span":{"begin":0,"end":108},"obj":"Sentence"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin-entities-OrganismTaxon-PD
{"project":"LitCoin-entities-OrganismTaxon-PD","denotations":[{"id":"T1","span":{"begin":77,"end":83},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"NCBItxid:12939"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin-entities
{"project":"LitCoin-entities","denotations":[{"id":"8851","span":{"begin":53,"end":58},"obj":"GeneOrGeneProduct"},{"id":"8852","span":{"begin":77,"end":83},"obj":"DiseaseOrPhenotypicFeature"},{"id":"8853","span":{"begin":85,"end":98},"obj":"DiseaseOrPhenotypicFeature"},{"id":"8854","span":{"begin":104,"end":107},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"db_id","subj":"8851","obj":"NCBIGene:5972"},{"id":"A2","pred":"db_id","subj":"8852","obj":"MESH:D000740"},{"id":"A3","pred":"db_id","subj":"8853","obj":"MESH:D033461"},{"id":"A4","pred":"db_id","subj":"8854","obj":"MESH:D051436"}],"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":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin_Mondo
{"project":"LitCoin_Mondo","denotations":[{"id":"T1","span":{"begin":77,"end":83},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0002280"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin-GeneOrGeneProduct-v0
{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T1","span":{"begin":19,"end":27},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":35,"end":49},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":53,"end":58},"obj":"GeneOrGeneProduct"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin-GeneOrGeneProduct-v2
{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":35,"end":49},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":53,"end":58},"obj":"GeneOrGeneProduct"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin-Disease-MeSH
{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":77,"end":83},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":85,"end":98},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":104,"end":107},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"originalLabel","subj":"T1","obj":"D000740"},{"id":"A2","pred":"originalLabel","subj":"T2","obj":"D033461"},{"id":"A3","pred":"originalLabel","subj":"T3","obj":"D051436"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin-GeneOrGeneProduct-v3
{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":35,"end":49},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":53,"end":58},"obj":"GeneOrGeneProduct"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin_Mondo_095
{"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":77,"end":83},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":104,"end":107},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0002280"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0005300"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin-MeSH-Disease-2
{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":77,"end":83},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":85,"end":98},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":104,"end":107},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D000740"},{"id":"A2","pred":"ID:","subj":"T2","obj":"D033461"},{"id":"A3","pred":"ID:","subj":"T3","obj":"D051436"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin-MONDO_bioort2019
{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":77,"end":83},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":85,"end":98},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":104,"end":107},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"D000740"},{"id":"A2","pred":"#label","subj":"T2","obj":"D033461"},{"id":"A3","pred":"#label","subj":"T3","obj":"D051436"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin-Chemical-MeSH-CHEBI
{"project":"LitCoin-Chemical-MeSH-CHEBI","denotations":[{"id":"T1","span":{"begin":53,"end":58},"obj":"ChemicalEntity"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D012083"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
LitCoin-training-merged
{"project":"LitCoin-training-merged","denotations":[{"id":"T1","span":{"begin":53,"end":58},"obj":"ChemicalEntity"},{"id":"T60777","span":{"begin":53,"end":58},"obj":"GeneOrGeneProduct"},{"id":"T16831","span":{"begin":35,"end":49},"obj":"GeneOrGeneProduct"},{"id":"T55177","span":{"begin":104,"end":107},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T15051","span":{"begin":85,"end":98},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T87390","span":{"begin":77,"end":83},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D012083"},{"id":"A96519","pred":"#label","subj":"T55177","obj":"D051436"},{"id":"A30549","pred":"#label","subj":"T15051","obj":"D033461"},{"id":"A54665","pred":"#label","subj":"T87390","obj":"D000740"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
sentences
{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":108},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":108},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
DisGeNET5_gene_disease
{"project":"DisGeNET5_gene_disease","denotations":[{"id":"21903317-0#53#58#gene5972","span":{"begin":53,"end":58},"obj":"gene5972"},{"id":"21903317-0#77#83#diseaseC0002871","span":{"begin":77,"end":83},"obj":"diseaseC0002871"},{"id":"21903317-0#104#107#diseaseC1561643","span":{"begin":104,"end":107},"obj":"diseaseC1561643"}],"relations":[{"id":"53#58#gene597277#83#diseaseC0002871","pred":"associated_with","subj":"21903317-0#53#58#gene5972","obj":"21903317-0#77#83#diseaseC0002871"},{"id":"53#58#gene5972104#107#diseaseC1561643","pred":"associated_with","subj":"21903317-0#53#58#gene5972","obj":"21903317-0#104#107#diseaseC1561643"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}
PubCasesHPO
{"project":"PubCasesHPO","denotations":[{"id":"TI1","span":{"begin":77,"end":83},"obj":"HP:0001903"},{"id":"TI2","span":{"begin":85,"end":98},"obj":"HP:0002149"}],"text":"Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD."}