PubMed:26900322 JSONTXT 26 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue db_id
11062 0-3 GeneOrGeneProduct denotes CFI NCBIGene:3426
11063 4-13 SequenceVariant denotes rs7356506 DBSNP:rs7356506
11064 44-73 DiseaseOrPhenotypicFeature denotes Vogt-Koyanagi-Harada syndrome MESH:D014607
11065 84-103 GeneOrGeneProduct denotes Complement factor I NCBIGene:3426
11066 105-108 GeneOrGeneProduct denotes CFI NCBIGene:3426
11067 210-217 DiseaseOrPhenotypicFeature denotes uveitis MESH:D014605
11068 306-309 GeneOrGeneProduct denotes CFI NCBIGene:3426
11069 336-371 DiseaseOrPhenotypicFeature denotes Vogt-Koyanagi-Harada (VKH) syndrome MESH:D014607
11070 397-405 OrganismTaxon denotes patients NCBITaxon:9606
11071 421-433 DiseaseOrPhenotypicFeature denotes VKH syndrome MESH:D014607
11072 575-578 GeneOrGeneProduct denotes CFI NCBIGene:3426
11073 579-588 SequenceVariant denotes rs7356506 DBSNP:rs7356506
11074 709-717 OrganismTaxon denotes patients NCBITaxon:9606
11075 813-821 DiseaseOrPhenotypicFeature denotes cataract MESH:D002386
11076 834-841 ChemicalEntity denotes steroid MESH:D013256
11077 914-917 GeneOrGeneProduct denotes CFI NCBIGene:3426
11078 918-927 SequenceVariant denotes rs7356506 DBSNP:rs7356506
11079 946-958 DiseaseOrPhenotypicFeature denotes VKH syndrome MESH:D014607
11080 969-977 OrganismTaxon denotes patients NCBITaxon:9606
11081 993-1005 DiseaseOrPhenotypicFeature denotes VKH syndrome MESH:D014607
11082 1067-1070 GeneOrGeneProduct denotes CFI NCBIGene:3426
11083 1071-1080 SequenceVariant denotes rs7356506 DBSNP:rs7356506
11084 1344-1347 GeneOrGeneProduct denotes CFI NCBIGene:3426
11085 1348-1357 SequenceVariant denotes rs7356506 DBSNP:rs7356506
11086 1361-1369 OrganismTaxon denotes patients NCBITaxon:9606
11087 1375-1387 DiseaseOrPhenotypicFeature denotes VKH syndrome MESH:D014607
11088 1405-1413 DiseaseOrPhenotypicFeature denotes cataract MESH:D002386
11089 1579-1587 OrganismTaxon denotes patients NCBITaxon:9606
11090 1593-1605 DiseaseOrPhenotypicFeature denotes VKH syndrome MESH:D014607
11091 1609-1616 ChemicalEntity denotes steroid MESH:D013256
11092 1653-1656 GeneOrGeneProduct denotes CFI NCBIGene:3426
11093 1657-1666 SequenceVariant denotes rs7356506 DBSNP:rs7356506
11094 1721-1724 GeneOrGeneProduct denotes CFI NCBIGene:3426
11095 1777-1789 DiseaseOrPhenotypicFeature denotes VKH syndrome MESH:D014607
11096 1850-1853 GeneOrGeneProduct denotes CFI NCBIGene:3426
11097 1854-1861 SequenceVariant denotes 7356506 DBSNP:rs7356506
11098 1867-1879 DiseaseOrPhenotypicFeature denotes VKH syndrome MESH:D014607
11099 1937-1945 DiseaseOrPhenotypicFeature denotes cataract MESH:D002386
11100 1968-1975 ChemicalEntity denotes steroid MESH:D013256