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PubMed:19208385 / 0-167
Annnotations
LitCoin-sentences
{"project":"LitCoin-sentences","denotations":[{"id":"T1","span":{"begin":0,"end":127},"obj":"Sentence"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
LitCoin-entities
{"project":"LitCoin-entities","denotations":[{"id":"5776","span":{"begin":0,"end":32},"obj":"DiseaseOrPhenotypicFeature"},{"id":"5777","span":{"begin":38,"end":61},"obj":"DiseaseOrPhenotypicFeature"},{"id":"5778","span":{"begin":66,"end":79},"obj":"DiseaseOrPhenotypicFeature"},{"id":"5779","span":{"begin":120,"end":126},"obj":"GeneOrGeneProduct"},{"id":"5780","span":{"begin":128,"end":151},"obj":"DiseaseOrPhenotypicFeature"},{"id":"5781","span":{"begin":153,"end":155},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"db_id","subj":"5776","obj":"MESH:C536044"},{"id":"A2","pred":"db_id","subj":"5777","obj":"MESH:D020300"},{"id":"A3","pred":"db_id","subj":"5778","obj":"MESH:D059327"},{"id":"A4","pred":"db_id","subj":"5779","obj":"NCBIGene:1278"},{"id":"A5","pred":"db_id","subj":"5780","obj":"MESH:D010013"},{"id":"A6","pred":"db_id","subj":"5781","obj":"MESH:D010013"}],"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":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
LitCoin_Mondo
{"project":"LitCoin_Mondo","denotations":[{"id":"T1","span":{"begin":0,"end":23},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":38,"end":61},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":66,"end":79},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":128,"end":151},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0019019"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0005049"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0021004"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0019019"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
LitCoin-GeneOrGeneProduct-v0
{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T1","span":{"begin":29,"end":32},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":96,"end":105},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":120,"end":126},"obj":"GeneOrGeneProduct"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
LitCoin-GeneOrGeneProduct-v2
{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":120,"end":126},"obj":"GeneOrGeneProduct"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
LitCoin-Disease-MeSH
{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":0,"end":32},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":38,"end":61},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":66,"end":79},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":128,"end":151},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":153,"end":155},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"originalLabel","subj":"T1","obj":"C536044"},{"id":"A2","pred":"originalLabel","subj":"T2","obj":"D020300"},{"id":"A3","pred":"originalLabel","subj":"T3","obj":"D059327"},{"id":"A4","pred":"originalLabel","subj":"T4","obj":"D010013"},{"id":"A5","pred":"originalLabel","subj":"T5","obj":"D010013"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
LitCoin-GeneOrGeneProduct-v3
{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":120,"end":126},"obj":"GeneOrGeneProduct"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
LitCoin_Mondo_095
{"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":0,"end":32},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":38,"end":61},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":66,"end":79},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":128,"end":151},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":153,"end":155},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0009804"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0005049"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0021004"},{"id":"A4","pred":"mondo_id","subj":"T3","obj":"0017424"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0019019"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"0019019"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
LitCoin-MeSH-Disease-2
{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":0,"end":32},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":38,"end":61},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":66,"end":79},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":128,"end":151},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":153,"end":155},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"C536044"},{"id":"A2","pred":"ID:","subj":"T2","obj":"D020300"},{"id":"A3","pred":"ID:","subj":"T3","obj":"D059327"},{"id":"A4","pred":"ID:","subj":"T4","obj":"D010013"},{"id":"A5","pred":"ID:","subj":"T5","obj":"D010013"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
LitCoin-MONDO_bioort2019
{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":0,"end":32},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":38,"end":61},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":66,"end":79},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":128,"end":151},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":153,"end":155},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"C536044"},{"id":"A2","pred":"#label","subj":"T2","obj":"D020300"},{"id":"A3","pred":"#label","subj":"T3","obj":"D059327"},{"id":"A4","pred":"#label","subj":"T4","obj":"D010013"},{"id":"A5","pred":"#label","subj":"T5","obj":"D010013"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
LitCoin-training-merged
{"project":"LitCoin-training-merged","denotations":[{"id":"T57517","span":{"begin":120,"end":126},"obj":"GeneOrGeneProduct"},{"id":"T88966","span":{"begin":153,"end":155},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T73081","span":{"begin":128,"end":151},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T39072","span":{"begin":66,"end":79},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T85622","span":{"begin":38,"end":61},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T35891","span":{"begin":0,"end":32},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A25082","pred":"#label","subj":"T88966","obj":"D010013"},{"id":"A11954","pred":"#label","subj":"T73081","obj":"D010013"},{"id":"A6932","pred":"#label","subj":"T39072","obj":"D059327"},{"id":"A4715","pred":"#label","subj":"T85622","obj":"D020300"},{"id":"A56069","pred":"#label","subj":"T35891","obj":"C536044"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
sentences
{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":127},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":127},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
DisGeNET5_gene_disease
{"project":"DisGeNET5_gene_disease","denotations":[{"id":"19208385-0#120#126#gene1278","span":{"begin":120,"end":126},"obj":"gene1278"},{"id":"19208385-0#0#32#diseaseC0268362","span":{"begin":0,"end":32},"obj":"diseaseC0268362"}],"relations":[{"id":"120#126#gene12780#32#diseaseC0268362","pred":"associated_with","subj":"19208385-0#120#126#gene1278","obj":"19208385-0#0#32#diseaseC0268362"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
PubCasesHPO
{"project":"PubCasesHPO","denotations":[{"id":"TI1","span":{"begin":38,"end":61},"obj":"HP:0002170"},{"id":"TI2","span":{"begin":66,"end":79},"obj":"HP:0001156"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}
PubCasesORDO
{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":128,"end":151},"obj":"ORDO:666"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.\nOsteogenesis imperfecta (OI) is a herit"}