PubMed:21219851 / 183-331 JSONTXT

{"project":"LitCoin-sentences","denotations":[{"id":"T2","span":{"begin":0,"end":148},"obj":"Sentence"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"LitCoin-entities","denotations":[{"id":"8482","span":{"begin":0,"end":37},"obj":"DiseaseOrPhenotypicFeature"},{"id":"8483","span":{"begin":39,"end":43},"obj":"DiseaseOrPhenotypicFeature"},{"id":"8484","span":{"begin":46,"end":57},"obj":"DiseaseOrPhenotypicFeature"},{"id":"8485","span":{"begin":65,"end":92},"obj":"DiseaseOrPhenotypicFeature"},{"id":"8486","span":{"begin":103,"end":123},"obj":"GeneOrGeneProduct"},{"id":"8487","span":{"begin":130,"end":136},"obj":"GeneOrGeneProduct"}],"attributes":[{"id":"A2","pred":"db_id","subj":"8482","obj":"MESH:D004535"},{"id":"A3","pred":"db_id","subj":"8483","obj":"MESH:D004535"},{"id":"A4","pred":"db_id","subj":"8484","obj":"MESH:D004535"},{"id":"A5","pred":"db_id","subj":"8485","obj":"MESH:D030342"},{"id":"A6","pred":"db_id","subj":"8486","obj":"NCBIGene:1281"},{"id":"A7","pred":"db_id","subj":"8487","obj":"NCBIGene:1281"}],"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":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"LitCoin_Mondo","denotations":[{"id":"T2","span":{"begin":0,"end":37},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":0,"end":22},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0017314"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0020066"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T8","span":{"begin":14,"end":22},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":108,"end":111},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":112,"end":123},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":130,"end":136},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":138,"end":147},"obj":"GeneOrGeneProduct"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T5","span":{"begin":14,"end":22},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":112,"end":123},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":130,"end":136},"obj":"GeneOrGeneProduct"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T2","span":{"begin":0,"end":37},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":65,"end":92},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"originalLabel","subj":"T2","obj":"D004535"},{"id":"A3","pred":"originalLabel","subj":"T3","obj":"DISEASE"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":112,"end":123},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":130,"end":136},"obj":"GeneOrGeneProduct"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T3","span":{"begin":0,"end":37},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":39,"end":43},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0017314"},{"id":"A4","pred":"mondo_id","subj":"T3","obj":"0007524"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0017314"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T2","span":{"begin":0,"end":37},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":39,"end":43},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":46,"end":57},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":65,"end":92},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"ID:","subj":"T2","obj":"D004535"},{"id":"A3","pred":"ID:","subj":"T3","obj":"DISEASE"},{"id":"A4","pred":"ID:","subj":"T4","obj":"DISEASE"},{"id":"A5","pred":"ID:","subj":"T5","obj":"DISEASE"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T2","span":{"begin":0,"end":37},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":39,"end":43},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":46,"end":57},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":65,"end":92},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"#label","subj":"T2","obj":"D004535"},{"id":"A3","pred":"#label","subj":"T3","obj":"DISEASE"},{"id":"A4","pred":"#label","subj":"T4","obj":"DISEASE"},{"id":"A5","pred":"#label","subj":"T5","obj":"DISEASE"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T55142","span":{"begin":130,"end":136},"obj":"GeneOrGeneProduct"},{"id":"T57369","span":{"begin":112,"end":123},"obj":"GeneOrGeneProduct"},{"id":"T32104","span":{"begin":65,"end":92},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T35010","span":{"begin":46,"end":57},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T37080","span":{"begin":39,"end":43},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T64173","span":{"begin":0,"end":37},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A5","pred":"#label","subj":"T32104","obj":"DISEASE"},{"id":"A4","pred":"#label","subj":"T35010","obj":"DISEASE"},{"id":"A76591","pred":"#label","subj":"T37080","obj":"DISEASE"},{"id":"A1919","pred":"#label","subj":"T64173","obj":"D004535"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":130,"end":136},"obj":"gene:1281"},{"id":"T1","span":{"begin":0,"end":37},"obj":"disease:C0268338"},{"id":"T2","span":{"begin":130,"end":136},"obj":"gene:1281"},{"id":"T3","span":{"begin":39,"end":43},"obj":"disease:C0268338"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"},{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":65,"end":83},"obj":"HP_0000006"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"21219851-1#130#136#gene1281","span":{"begin":130,"end":136},"obj":"gene1281"},{"id":"21219851-1#0#37#diseaseC0268338","span":{"begin":0,"end":37},"obj":"diseaseC0268338"},{"id":"21219851-1#39#43#diseaseC0268338","span":{"begin":39,"end":43},"obj":"diseaseC0268338"}],"relations":[{"id":"130#136#gene12810#37#diseaseC0268338","pred":"associated_with","subj":"21219851-1#130#136#gene1281","obj":"21219851-1#0#37#diseaseC0268338"},{"id":"130#136#gene128139#43#diseaseC0268338","pred":"associated_with","subj":"21219851-1#130#136#gene1281","obj":"21219851-1#39#43#diseaseC0268338"}],"text":"Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by type III procollagen gene (COL3A1) mutations."}