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PubMed:17033974 JSONTXT 19 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label ID:
T14074 26-41 GeneOrGeneProduct denotes calcium-channel
T39385 50-58 GeneOrGeneProduct denotes CACNA2D4
T1 86-100 DiseaseOrPhenotypicFeature denotes cone dystrophy D000077765
T10600 102-109 ChemicalEntity denotes Retinal http://purl.obolibrary.org/obo/CHEBI_17898
T43972 183-199 GeneOrGeneProduct denotes calcium channels
T38311 217-223 GeneOrGeneProduct denotes ribbon
T43413 297-305 GeneOrGeneProduct denotes Cacna2d4
T79427 328-333 OrganismTaxon denotes mouse
T36328 363-370 ChemicalEntity denotes retinal http://purl.obolibrary.org/obo/CHEBI_15035|D012172
T80950 411-417 GeneOrGeneProduct denotes ribbon
T7 450-458 GeneOrGeneProduct denotes Cacna2d4
T8 482-497 GeneOrGeneProduct denotes calcium-channel
T9 523-528 GeneOrGeneProduct denotes alpha
T75998 533-538 OrganismTaxon denotes delta
T20409 562-567 OrganismTaxon denotes human
T10 580-588 GeneOrGeneProduct denotes CACNA2D4
T13510 679-687 OrganismTaxon denotes patients
T2 725-740 DiseaseOrPhenotypicFeature denotes night blindness D009755
T84447 825-830 SequenceVariant denotes 2406C
T11 839-847 GeneOrGeneProduct denotes CACNA2D4
T5 967-975 OrganismTaxon denotes patients
T3 1013-1027 DiseaseOrPhenotypicFeature denotes cone dystrophy D000077765
T6 1092-1097 OrganismTaxon denotes human
T12 1098-1106 GeneOrGeneProduct denotes CACNA2D4
T13 1125-1135 GeneOrGeneProduct denotes novel gene
T4 1175-1189 DiseaseOrPhenotypicFeature denotes cone dystrophy D000077765