PubMed:17059986 / 0-95
Annnotations
LitCoin-entities
{"project":"LitCoin-entities","denotations":[{"id":"3530","span":{"begin":29,"end":36},"obj":"GeneOrGeneProduct"},{"id":"3531","span":{"begin":53,"end":70},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"db_id","subj":"3530","obj":"NCBIGene:6559"},{"id":"A2","pred":"db_id","subj":"3531","obj":"MESH:D053579"}],"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":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
LitCoin_Mondo
{"project":"LitCoin_Mondo","denotations":[{"id":"T1","span":{"begin":53,"end":70},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":75,"end":85},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0009904"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0700005"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
LitCoin-GeneOrGeneProduct-v2
{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":2,"end":7},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":29,"end":36},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":62,"end":70},"obj":"GeneOrGeneProduct"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
LitCoin-GeneOrGeneProduct-v0
{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T1","span":{"begin":2,"end":7},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":8,"end":16},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":17,"end":25},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":29,"end":36},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":62,"end":70},"obj":"GeneOrGeneProduct"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
LitCoin-Disease-MeSH
{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":53,"end":70},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"originalLabel","subj":"T1","obj":"D053579"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
LitCoin-GeneOrGeneProduct-v3
{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":29,"end":36},"obj":"GeneOrGeneProduct"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
LitCoin_Mondo_095
{"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":53,"end":70},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0009904"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
LitCoin-MeSH-Disease-2
{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":53,"end":70},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D053579"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
LitCoin-MONDO_bioort2019
{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":53,"end":70},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"D053579"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
LitCoin-training-merged
{"project":"LitCoin-training-merged","denotations":[{"id":"T21958","span":{"begin":29,"end":36},"obj":"GeneOrGeneProduct"},{"id":"T73539","span":{"begin":53,"end":70},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A106","pred":"#label","subj":"T73539","obj":"D053579"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
DisGeNET
{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":29,"end":36},"obj":"gene:6559"},{"id":"T1","span":{"begin":53,"end":70},"obj":"disease:C0268450"},{"id":"T2","span":{"begin":29,"end":36},"obj":"gene:6559"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
DisGeNET5_gene_disease
{"project":"DisGeNET5_gene_disease","denotations":[{"id":"17059986-0#29#36#gene6559","span":{"begin":29,"end":36},"obj":"gene6559"},{"id":"17059986-0#53#70#diseaseC0268450","span":{"begin":53,"end":70},"obj":"diseaseC0268450"}],"relations":[{"id":"29#36#gene655953#70#diseaseC0268450","pred":"associated_with","subj":"17059986-0#29#36#gene6559","obj":"17059986-0#53#70#diseaseC0268450"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}
PubCasesORDO
{"project":"PubCasesORDO","denotations":[{"id":"TI1","span":{"begin":53,"end":70},"obj":"ORDO:358"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracran"}