
PubMed:17033974 / 234-445
Annnotations
TEST-ChemicalEntity
{"project":"TEST-ChemicalEntity","denotations":[{"id":"T8","span":{"begin":129,"end":136},"obj":"ChemicalEntity"}],"attributes":[{"id":"A8","pred":"ID:","subj":"T8","obj":"D012172"},{"id":"A9","pred":"ID:","subj":"T8","obj":"http://purl.obolibrary.org/obo/CHEBI_15035"}],"text":"We recently identified a truncating frameshift mutation in the Cacna2d4 gene in a spontaneous mouse mutant with profound loss of retinal signaling and an abnormal morphology of ribbon synapses in rods and cones."}
TEST-OrganismTaxon
{"project":"TEST-OrganismTaxon","denotations":[{"id":"T1","span":{"begin":94,"end":99},"obj":"OrganismTaxon"}],"text":"We recently identified a truncating frameshift mutation in the Cacna2d4 gene in a spontaneous mouse mutant with profound loss of retinal signaling and an abnormal morphology of ribbon synapses in rods and cones."}
Test-GeneOrGeneProduct
{"project":"Test-GeneOrGeneProduct","denotations":[{"id":"T5","span":{"begin":63,"end":71},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":177,"end":183},"obj":"GeneOrGeneProduct"}],"text":"We recently identified a truncating frameshift mutation in the Cacna2d4 gene in a spontaneous mouse mutant with profound loss of retinal signaling and an abnormal morphology of ribbon synapses in rods and cones."}
Test-merged-2
{"project":"Test-merged-2","denotations":[{"id":"T36328","span":{"begin":129,"end":136},"obj":"ChemicalEntity"},{"id":"T43413","span":{"begin":63,"end":71},"obj":"GeneOrGeneProduct"},{"id":"T80950","span":{"begin":177,"end":183},"obj":"GeneOrGeneProduct"},{"id":"T79427","span":{"begin":94,"end":99},"obj":"OrganismTaxon"}],"attributes":[{"id":"A8","pred":"ID:","subj":"T36328","obj":"D012172"},{"id":"A9","pred":"ID:","subj":"T36328","obj":"http://purl.obolibrary.org/obo/CHEBI_15035"}],"text":"We recently identified a truncating frameshift mutation in the Cacna2d4 gene in a spontaneous mouse mutant with profound loss of retinal signaling and an abnormal morphology of ribbon synapses in rods and cones."}
sentences
{"project":"sentences","denotations":[{"id":"TextSentencer_T3","span":{"begin":0,"end":211},"obj":"Sentence"},{"id":"T3","span":{"begin":0,"end":211},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"We recently identified a truncating frameshift mutation in the Cacna2d4 gene in a spontaneous mouse mutant with profound loss of retinal signaling and an abnormal morphology of ribbon synapses in rods and cones."}
PubmedHPO
{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":129,"end":162},"obj":"HP_0000479"},{"id":"T2","span":{"begin":129,"end":162},"obj":"HP_0007901"}],"text":"We recently identified a truncating frameshift mutation in the Cacna2d4 gene in a spontaneous mouse mutant with profound loss of retinal signaling and an abnormal morphology of ribbon synapses in rods and cones."}