PubMed:20682662 JSONTXT 29 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue db_id
7740 23-47 GeneOrGeneProduct denotes C-C chemokine receptor 5 NCBIGene:1234
7741 48-60 SequenceVariant denotes Δ32 deletion c|DEL||32
7742 73-93 DiseaseOrPhenotypicFeature denotes rheumatoid arthritis MESH:D001172
7743 95-123 DiseaseOrPhenotypicFeature denotes systemic lupus erythematosus MESH:D008180
7744 125-140 DiseaseOrPhenotypicFeature denotes lupus nephritis MESH:D008181
7745 175-199 GeneOrGeneProduct denotes C-C chemokine receptor 5 NCBIGene:1234
7746 201-205 GeneOrGeneProduct denotes CCR5 NCBIGene:1234
7747 234-246 DiseaseOrPhenotypicFeature denotes inflammation MESH:D007249
7748 250-277 SequenceVariant denotes 32 base-pair (Δ32) deletion c|DEL||32
7749 285-289 GeneOrGeneProduct denotes CCR5 NCBIGene:1234
7750 436-455 DiseaseOrPhenotypicFeature denotes autoimmune diseases MESH:D001327
7751 485-497 SequenceVariant denotes Δ32 deletion c|DEL||32
7752 559-567 OrganismTaxon denotes patients NCBITaxon:9606
7753 573-593 DiseaseOrPhenotypicFeature denotes rheumatoid arthritis MESH:D001172
7754 595-597 DiseaseOrPhenotypicFeature denotes RA MESH:D001172
7755 600-628 DiseaseOrPhenotypicFeature denotes systemic lupus erythematosus MESH:D008180
7756 630-633 DiseaseOrPhenotypicFeature denotes SLE MESH:D008180
7757 640-655 DiseaseOrPhenotypicFeature denotes lupus nephritis MESH:D008181
7758 657-659 DiseaseOrPhenotypicFeature denotes LN MESH:D008181
7759 744-746 DiseaseOrPhenotypicFeature denotes RA MESH:D001172
7760 747-755 OrganismTaxon denotes patients NCBITaxon:9606
7761 760-763 DiseaseOrPhenotypicFeature denotes SLE MESH:D008180
7762 764-772 OrganismTaxon denotes patients NCBITaxon:9606
7763 778-780 DiseaseOrPhenotypicFeature denotes LN MESH:D008181
7764 781-789 OrganismTaxon denotes patients NCBITaxon:9606
7765 839-843 GeneOrGeneProduct denotes CCR5 NCBIGene:1234
7766 844-856 SequenceVariant denotes Δ32 deletion c|DEL||32
7767 914-922 OrganismTaxon denotes patients NCBITaxon:9606
7768 1106-1114 OrganismTaxon denotes patients NCBITaxon:9606
7769 1159-1163 GeneOrGeneProduct denotes CCR5 NCBIGene:1234
7770 1164-1167 SequenceVariant denotes Δ32 c|DEL||32
7771 1169-1172 SequenceVariant denotes Δ32 c|DEL||32
7772 1173-1176 SequenceVariant denotes Δ32 c|DEL||32
7773 1178-1180 DiseaseOrPhenotypicFeature denotes RA MESH:D001172
7774 1211-1214 DiseaseOrPhenotypicFeature denotes SLE MESH:D008180
7775 1231-1233 DiseaseOrPhenotypicFeature denotes LN MESH:D008181
7776 1313-1325 SequenceVariant denotes Δ32 deletion c|DEL||32
7777 1346-1348 DiseaseOrPhenotypicFeature denotes LN MESH:D008181
7778 1349-1357 OrganismTaxon denotes patients NCBITaxon:9606
7779 1440-1444 GeneOrGeneProduct denotes CCR5 NCBIGene:1234
7780 1476-1478 DiseaseOrPhenotypicFeature denotes RA MESH:D001172
7781 1480-1483 DiseaseOrPhenotypicFeature denotes SLE MESH:D008180
7782 1488-1490 DiseaseOrPhenotypicFeature denotes LN MESH:D008181
7783 1533-1535 DiseaseOrPhenotypicFeature denotes LN MESH:D008181
7784 1560-1564 GeneOrGeneProduct denotes CCR5 NCBIGene:1234
7785 1565-1577 SequenceVariant denotes Δ32 deletion c|DEL||32
7786 1636-1638 DiseaseOrPhenotypicFeature denotes RA MESH:D001172
7787 1640-1643 DiseaseOrPhenotypicFeature denotes SLE MESH:D008180
7788 1648-1650 DiseaseOrPhenotypicFeature denotes LN MESH:D008181
7789 1681-1693 SequenceVariant denotes Δ32 deletion c|DEL||32