PubMed:17033686 / 388-580 JSONTXT

{"project":"LitCoin-sentences","denotations":[{"id":"T3","span":{"begin":0,"end":192},"obj":"Sentence"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"LitCoin-entities","denotations":[{"id":"3456","span":{"begin":56,"end":96},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3457","span":{"begin":98,"end":100},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3458","span":{"begin":103,"end":117},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3459","span":{"begin":119,"end":135},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3460","span":{"begin":137,"end":149},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3461","span":{"begin":151,"end":167},"obj":"DiseaseOrPhenotypicFeature"},{"id":"3462","span":{"begin":173,"end":191},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A11","pred":"db_id","subj":"3456","obj":"MESH:D038901"},{"id":"A12","pred":"db_id","subj":"3457","obj":"MESH:D008607"},{"id":"A13","pred":"db_id","subj":"3458","obj":"MESH:D008850"},{"id":"A14","pred":"db_id","subj":"3459","obj":"MESH:D003103"},{"id":"A15","pred":"db_id","subj":"3460","obj":"MESH:D008831"},{"id":"A16","pred":"db_id","subj":"3461","obj":"MESH:D007674"},{"id":"A17","pred":"db_id","subj":"3462","obj":"MESH:D010264"}],"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":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"LitCoin_Mondo","denotations":[{"id":"T3","span":{"begin":103,"end":117},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":119,"end":126},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":127,"end":135},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":137,"end":149},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T7","span":{"begin":151,"end":167},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8","span":{"begin":181,"end":191},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0021129"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0001280"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0001476"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"0001149"},{"id":"A7","pred":"mondo_id","subj":"T7","obj":"0019637"},{"id":"A8","pred":"mondo_id","subj":"T8","obj":"0003757"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T15","span":{"begin":56,"end":64},"obj":"GeneOrGeneProduct"},{"id":"T16","span":{"begin":103,"end":117},"obj":"GeneOrGeneProduct"},{"id":"T17","span":{"begin":173,"end":180},"obj":"GeneOrGeneProduct"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T9","span":{"begin":56,"end":64},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":103,"end":117},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":173,"end":180},"obj":"GeneOrGeneProduct"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T7","span":{"begin":78,"end":96},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8","span":{"begin":98,"end":100},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":103,"end":117},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":127,"end":135},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":137,"end":149},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":173,"end":191},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A7","pred":"originalLabel","subj":"T7","obj":"D008607"},{"id":"A8","pred":"originalLabel","subj":"T8","obj":"D008607"},{"id":"A9","pred":"originalLabel","subj":"T9","obj":"D008850"},{"id":"A10","pred":"originalLabel","subj":"T10","obj":"D003103"},{"id":"A11","pred":"originalLabel","subj":"T11","obj":"D008831"},{"id":"A12","pred":"originalLabel","subj":"T12","obj":"D010264"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T8","span":{"begin":78,"end":96},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":98,"end":100},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":103,"end":117},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":127,"end":135},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":137,"end":149},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T13","span":{"begin":151,"end":167},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T14","span":{"begin":173,"end":191},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"mondo_id","subj":"T8","obj":"0001071"},{"id":"A9","pred":"mondo_id","subj":"T9","obj":"0001071"},{"id":"A10","pred":"mondo_id","subj":"T10","obj":"0021129"},{"id":"A11","pred":"mondo_id","subj":"T11","obj":"0001476"},{"id":"A12","pred":"mondo_id","subj":"T12","obj":"0001149"},{"id":"A13","pred":"mondo_id","subj":"T13","obj":"0019637"},{"id":"A14","pred":"mondo_id","subj":"T14","obj":"0019064"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T9","span":{"begin":56,"end":96},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":98,"end":100},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":103,"end":117},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":127,"end":135},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T13","span":{"begin":137,"end":149},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T14","span":{"begin":151,"end":167},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T15","span":{"begin":173,"end":191},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A9","pred":"ID:","subj":"T9","obj":"DISEASE"},{"id":"A10","pred":"ID:","subj":"T10","obj":"D008607"},{"id":"A11","pred":"ID:","subj":"T11","obj":"D008850"},{"id":"A12","pred":"ID:","subj":"T12","obj":"D003103"},{"id":"A13","pred":"ID:","subj":"T13","obj":"D008831"},{"id":"A14","pred":"ID:","subj":"T14","obj":"DISEASE"},{"id":"A15","pred":"ID:","subj":"T15","obj":"D010264"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T9","span":{"begin":56,"end":96},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":98,"end":100},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":103,"end":117},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":127,"end":135},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T13","span":{"begin":137,"end":149},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T14","span":{"begin":151,"end":167},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T15","span":{"begin":173,"end":191},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A9","pred":"#label","subj":"T9","obj":"DISEASE"},{"id":"A10","pred":"#label","subj":"T10","obj":"D008607"},{"id":"A11","pred":"#label","subj":"T11","obj":"D008850"},{"id":"A12","pred":"#label","subj":"T12","obj":"D003103"},{"id":"A13","pred":"#label","subj":"T13","obj":"D008831"},{"id":"A14","pred":"#label","subj":"T14","obj":"DISEASE"},{"id":"A15","pred":"#label","subj":"T15","obj":"D010264"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T15","span":{"begin":173,"end":191},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T14","span":{"begin":151,"end":167},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T13","span":{"begin":137,"end":149},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":127,"end":135},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":103,"end":117},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":98,"end":100},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T96765","span":{"begin":56,"end":96},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A15","pred":"#label","subj":"T15","obj":"D010264"},{"id":"A14","pred":"#label","subj":"T14","obj":"DISEASE"},{"id":"A13","pred":"#label","subj":"T13","obj":"D008831"},{"id":"A12","pred":"#label","subj":"T12","obj":"D003103"},{"id":"A11","pred":"#label","subj":"T11","obj":"D008850"},{"id":"A10","pred":"#label","subj":"T10","obj":"D008607"},{"id":"A9","pred":"#label","subj":"T96765","obj":"DISEASE"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T3","span":{"begin":0,"end":192},"obj":"Sentence"},{"id":"T3","span":{"begin":0,"end":192},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"PubmedHPO","denotations":[{"id":"T3","span":{"begin":56,"end":64},"obj":"HP_0001417"},{"id":"T4","span":{"begin":78,"end":96},"obj":"HP_0001249"},{"id":"T5","span":{"begin":103,"end":117},"obj":"HP_0000568"},{"id":"T6","span":{"begin":119,"end":135},"obj":"HP_0000611"},{"id":"T7","span":{"begin":127,"end":135},"obj":"HP_0000589"},{"id":"T8","span":{"begin":137,"end":149},"obj":"HP_0000252"},{"id":"T9","span":{"begin":151,"end":167},"obj":"HP_0000089"},{"id":"T10","span":{"begin":173,"end":180},"obj":"HP_0001257"},{"id":"T11","span":{"begin":173,"end":191},"obj":"HP_0001258"},{"id":"T12","span":{"begin":181,"end":191},"obj":"HP_0010550"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"PubCasesHPO","denotations":[{"id":"AB1","span":{"begin":103,"end":117},"obj":"HP:0000568"},{"id":"AB2","span":{"begin":127,"end":135},"obj":"HP:0000589"},{"id":"AB3","span":{"begin":137,"end":149},"obj":"HP:0000252"},{"id":"AB4","span":{"begin":151,"end":167},"obj":"HP:0000089"},{"id":"AB5","span":{"begin":173,"end":191},"obj":"HP:0001258"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}

{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":151,"end":167},"obj":"ORDO:93101"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Here, we report two maternal cousins with an apparently X-linked phenotype of mental retardation (MR), microphthalmia, choroid coloboma, microcephaly, renal hypoplasia, and spastic paraplegia."}