PubMed:2063924 JSONTXT

{"project":"LitCoin-PubTator-for-Tuning","denotations":[{"id":"3","span":{"begin":37,"end":51},"obj":"GeneOrGeneProduct"},{"id":"4","span":{"begin":61,"end":69},"obj":"OrganismTaxon"},{"id":"5","span":{"begin":75,"end":99},"obj":"DiseaseOrPhenotypicFeature"},{"id":"12","span":{"begin":131,"end":139},"obj":"OrganismTaxon"},{"id":"13","span":{"begin":145,"end":169},"obj":"DiseaseOrPhenotypicFeature"},{"id":"14","span":{"begin":251,"end":265},"obj":"GeneOrGeneProduct"},{"id":"15","span":{"begin":267,"end":271},"obj":"GeneOrGeneProduct"},{"id":"16","span":{"begin":389,"end":393},"obj":"GeneOrGeneProduct"},{"id":"17","span":{"begin":405,"end":413},"obj":"OrganismTaxon"}],"attributes":[{"id":"A4","pred":"tao:has_database_id","subj":"4","obj":"Tax:9606"},{"id":"A13","pred":"tao:has_database_id","subj":"13","obj":"MESH:D012175"},{"id":"A12","pred":"tao:has_database_id","subj":"12","obj":"Tax:9606"},{"id":"A5","pred":"tao:has_database_id","subj":"5","obj":"MESH:D012175"},{"id":"A14","pred":"tao:has_database_id","subj":"14","obj":"Gene:5925"},{"id":"A15","pred":"tao:has_database_id","subj":"15","obj":"Gene:5925"},{"id":"A3","pred":"tao:has_database_id","subj":"3","obj":"Gene:5925"},{"id":"A17","pred":"tao:has_database_id","subj":"17","obj":"Tax:9606"},{"id":"A16","pred":"tao:has_database_id","subj":"16","obj":"Gene:5925"}],"text":"Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma.\nDNA samples from 92 unrelated patients with bilateral retinoblastoma were analyzed by Southern blot hybridization with cDNA and genomic clones of the retinoblastoma (RB-1) gene. Qualitative and quantitative evaluation of the Southern blot patterns showed a deletion of all or part of the RB-1 gene in 15 patients. Deletion hot spots were not detected. The study shows that 16% of germ cell mutations are detectable by Southern blot hybridization, but that densitometric analysis is required in most cases."}

{"project":"LitCoin-Disease-Tuning-1","denotations":[{"id":"T1","span":{"begin":37,"end":51},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":85,"end":99},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":155,"end":169},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":251,"end":265},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D012175"},{"id":"A2","pred":"ID:","subj":"T2","obj":"D012175"},{"id":"A3","pred":"ID:","subj":"T3","obj":"D012175"},{"id":"A4","pred":"ID:","subj":"T4","obj":"D012175"}],"text":"Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma.\nDNA samples from 92 unrelated patients with bilateral retinoblastoma were analyzed by Southern blot hybridization with cDNA and genomic clones of the retinoblastoma (RB-1) gene. Qualitative and quantitative evaluation of the Southern blot patterns showed a deletion of all or part of the RB-1 gene in 15 patients. Deletion hot spots were not detected. The study shows that 16% of germ cell mutations are detectable by Southern blot hybridization, but that densitometric analysis is required in most cases."}

{"project":"LitCoin-PubTator-for-Tuning-SeqVar","denotations":[{"id":"T1","span":{"begin":358,"end":373},"obj":"SequenceVariant"}],"text":"Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma.\nDNA samples from 92 unrelated patients with bilateral retinoblastoma were analyzed by Southern blot hybridization with cDNA and genomic clones of the retinoblastoma (RB-1) gene. Qualitative and quantitative evaluation of the Southern blot patterns showed a deletion of all or part of the RB-1 gene in 15 patients. Deletion hot spots were not detected. The study shows that 16% of germ cell mutations are detectable by Southern blot hybridization, but that densitometric analysis is required in most cases."}

{"project":"LitEisuke","denotations":[{"id":"T1","span":{"begin":37,"end":51},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":85,"end":99},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":155,"end":169},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":251,"end":265},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"D012175"},{"id":"A2","pred":"#label","subj":"T2","obj":"D012175"},{"id":"A3","pred":"#label","subj":"T3","obj":"D012175"},{"id":"A4","pred":"#label","subj":"T4","obj":"D012175"}],"text":"Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma.\nDNA samples from 92 unrelated patients with bilateral retinoblastoma were analyzed by Southern blot hybridization with cDNA and genomic clones of the retinoblastoma (RB-1) gene. Qualitative and quantitative evaluation of the Southern blot patterns showed a deletion of all or part of the RB-1 gene in 15 patients. Deletion hot spots were not detected. The study shows that 16% of germ cell mutations are detectable by Southern blot hybridization, but that densitometric analysis is required in most cases."}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":267,"end":271},"obj":"gene:5925"},{"id":"T1","span":{"begin":145,"end":169},"obj":"disease:C0854914"},{"id":"T2","span":{"begin":267,"end":271},"obj":"gene:129831"},{"id":"T3","span":{"begin":145,"end":169},"obj":"disease:C0854914"}],"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":"Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma.\nDNA samples from 92 unrelated patients with bilateral retinoblastoma were analyzed by Southern blot hybridization with cDNA and genomic clones of the retinoblastoma (RB-1) gene. Qualitative and quantitative evaluation of the Southern blot patterns showed a deletion of all or part of the RB-1 gene in 15 patients. Deletion hot spots were not detected. The study shows that 16% of germ cell mutations are detectable by Southern blot hybridization, but that densitometric analysis is required in most cases."}

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":155,"end":169},"obj":"HP_0009919"},{"id":"T2","span":{"begin":251,"end":265},"obj":"HP_0009919"}],"text":"Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma.\nDNA samples from 92 unrelated patients with bilateral retinoblastoma were analyzed by Southern blot hybridization with cDNA and genomic clones of the retinoblastoma (RB-1) gene. Qualitative and quantitative evaluation of the Southern blot patterns showed a deletion of all or part of the RB-1 gene in 15 patients. Deletion hot spots were not detected. The study shows that 16% of germ cell mutations are detectable by Southern blot hybridization, but that densitometric analysis is required in most cases."}