PubMed:16288197 JSONTXT 29 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label ID:
T76097 34-55 DiseaseOrPhenotypicFeature denotes congenital microcoria C537550
T88181 99-120 DiseaseOrPhenotypicFeature denotes Congenital microcoria C537550
T17575 180-184 OrganismTaxon denotes iris
T1006 201-207 DiseaseOrPhenotypicFeature denotes myopia D009216
T89176 212-220 GeneOrGeneProduct denotes juvenile
T16291 221-240 DiseaseOrPhenotypicFeature denotes open angle glaucoma D005902
T99309 409-430 DiseaseOrPhenotypicFeature denotes congenital microcoria C537550
T76489 1182-1203 DiseaseOrPhenotypicFeature denotes congenital microcoria C537550
T56881 1286-1296 DiseaseOrPhenotypicFeature denotes microcoria DISEASE
T7748 1301-1309 DiseaseOrPhenotypicFeature denotes glaucoma D005901
T90156 1328-1336 DiseaseOrPhenotypicFeature denotes glaucoma D005901
T73887 1344-1352 GeneOrGeneProduct denotes myocilin
T3 1354-1358 GeneOrGeneProduct denotes MYOC
T4 1361-1371 GeneOrGeneProduct denotes optineurin
T5 1373-1377 GeneOrGeneProduct denotes OPTN
T6 1383-1389 GeneOrGeneProduct denotes CYP1B1
T58359 1457-1461 SequenceVariant denotes Q48H
T7 1492-1496 GeneOrGeneProduct denotes MYOC
T85454 1536-1544 DiseaseOrPhenotypicFeature denotes glaucoma D005901
T64874 1545-1553 OrganismTaxon denotes patients
T51072 1675-1696 DiseaseOrPhenotypicFeature denotes congenital microcoria C537550
T8 1704-1708 GeneOrGeneProduct denotes MCOR
T9 1946-1950 GeneOrGeneProduct denotes MCOR
T1 2037-2047 ChemicalEntity denotes tyrosinase D014442
T10 2037-2047 GeneOrGeneProduct denotes tyrosinase
T3039 2067-2079 DiseaseOrPhenotypicFeature denotes pigmentation DISEASE
T13 2155-2176 DiseaseOrPhenotypicFeature denotes congenital microcoria C537550
T14 2208-2216 DiseaseOrPhenotypicFeature denotes glaucoma D005901
T11 2289-2293 GeneOrGeneProduct denotes MYOC
T90869 2294-2298 SequenceVariant denotes Q48H
T15 2354-2362 DiseaseOrPhenotypicFeature denotes glaucoma D005901
T2 2482-2486 ChemicalEntity denotes lead D007854
T16 2516-2526 DiseaseOrPhenotypicFeature denotes microcoria DISEASE
T17 2531-2539 DiseaseOrPhenotypicFeature denotes glaucoma D005901
T18 2576-2586 DiseaseOrPhenotypicFeature denotes microcoria DISEASE
T19 2588-2596 DiseaseOrPhenotypicFeature denotes glaucoma D005901
T12 2606-2610 GeneOrGeneProduct denotes MYOC
T56255 2611-2615 SequenceVariant denotes Q48H