PubMed:11558822 / 134-318 JSONTXT

{"project":"FSU-PRGE","denotations":[{"id":"T3","span":{"begin":149,"end":169},"obj":"protein"},{"id":"T4","span":{"begin":171,"end":177},"obj":"protein"}],"text":"To describe three patients with congenital glaucoma homozygous and compound heterozygous for different mutations and benign sequence variants in the cytochrome P 450 1B1 (CYP1B1) gene."}

{"project":"PIR-corpus2","denotations":[{"id":"T3","span":{"begin":149,"end":178},"obj":"protein"}],"text":"To describe three patients with congenital glaucoma homozygous and compound heterozygous for different mutations and benign sequence variants in the cytochrome P 450 1B1 (CYP1B1) gene."}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"11558822-1#171#177#gene1545","span":{"begin":171,"end":177},"obj":"gene1545"},{"id":"11558822-1#32#51#diseaseC0020302","span":{"begin":32,"end":51},"obj":"diseaseC0020302"}],"relations":[{"id":"171#177#gene154532#51#diseaseC0020302","pred":"associated_with","subj":"11558822-1#171#177#gene1545","obj":"11558822-1#32#51#diseaseC0020302"}],"text":"To describe three patients with congenital glaucoma homozygous and compound heterozygous for different mutations and benign sequence variants in the cytochrome P 450 1B1 (CYP1B1) gene."}

{"project":"PubCasesHPO","denotations":[{"id":"AB1","span":{"begin":32,"end":51},"obj":"HP:0001087"}],"text":"To describe three patients with congenital glaucoma homozygous and compound heterozygous for different mutations and benign sequence variants in the cytochrome P 450 1B1 (CYP1B1) gene."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T3","span":{"begin":0,"end":184},"obj":"Sentence"},{"id":"T3","span":{"begin":0,"end":184},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"To describe three patients with congenital glaucoma homozygous and compound heterozygous for different mutations and benign sequence variants in the cytochrome P 450 1B1 (CYP1B1) gene."}

{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":32,"end":51},"obj":"ORDO:98976"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"To describe three patients with congenital glaucoma homozygous and compound heterozygous for different mutations and benign sequence variants in the cytochrome P 450 1B1 (CYP1B1) gene."}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":149,"end":165},"obj":"gene:4051"},{"id":"T1","span":{"begin":32,"end":51},"obj":"disease:C0020302"},{"id":"T2","span":{"begin":171,"end":177},"obj":"gene:1545"},{"id":"T3","span":{"begin":32,"end":51},"obj":"disease:C0020302"}],"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":"To describe three patients with congenital glaucoma homozygous and compound heterozygous for different mutations and benign sequence variants in the cytochrome P 450 1B1 (CYP1B1) gene."}