PubMed:18366737 JSONTXT 26 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
4833 4-6 GeneOrGeneProduct denotes FH NCBIGene:2271
4834 48-66 GeneOrGeneProduct denotes fumarate hydratase NCBIGene:2271
4835 93-97 DiseaseOrPhenotypicFeature denotes MCUL MESH:C535516
4836 99-104 DiseaseOrPhenotypicFeature denotes HLRCC MESH:C535516
4837 106-120 DiseaseOrPhenotypicFeature denotes tumor syndrome MESH:D009369
4838 136-155 DiseaseOrPhenotypicFeature denotes fumarase deficiency MESH:C538191
4839 169-187 GeneOrGeneProduct denotes Fumarate hydratase NCBIGene:2271
4840 217-219 GeneOrGeneProduct denotes FH NCBIGene:2271
4841 236-244 GeneOrGeneProduct denotes fumarase NCBIGene:2271
4842 266-284 ChemicalEntity denotes tricarboxylic acid MESH:D014233
4843 286-289 ChemicalEntity denotes TCA MESH:D014233
4844 389-405 DiseaseOrPhenotypicFeature denotes deficiency of FH MESH:C538191
4845 437-451 DiseaseOrPhenotypicFeature denotes encephalopathy MESH:D001927
4846 475-484 DiseaseOrPhenotypicFeature denotes Leiomyoma MESH:D007889
4847 542-544 GeneOrGeneProduct denotes FH NCBIGene:2271
4848 548-556 OrganismTaxon denotes patients NCBITaxon:9606
4849 562-603 DiseaseOrPhenotypicFeature denotes multiple cutaneous and uterine leiomyomas MESH:C535516
4850 606-610 DiseaseOrPhenotypicFeature denotes MCUL MESH:C535516
4851 612-623 DiseaseOrPhenotypicFeature denotes OMIM 150800 MESH:C535516
4852 643-660 DiseaseOrPhenotypicFeature denotes renal cell cancer MESH:D002292
4853 733-780 DiseaseOrPhenotypicFeature denotes hereditary leiomyomatosis and renal cell cancer MESH:C535516
4854 782-787 DiseaseOrPhenotypicFeature denotes HLRCC MESH:C535516
4855 789-800 DiseaseOrPhenotypicFeature denotes OMIM 605839 MESH:C535516
4856 825-827 GeneOrGeneProduct denotes FH NCBIGene:2271
4857 833-838 DiseaseOrPhenotypicFeature denotes tumor MESH:D009369
4858 1060-1073 DiseaseOrPhenotypicFeature denotes tumorigenesis MESH:D009369
4859 1092-1094 GeneOrGeneProduct denotes FH NCBIGene:2271
4860 1130-1133 ChemicalEntity denotes TCA MESH:D014233
4861 1444-1446 GeneOrGeneProduct denotes FH NCBIGene:2271
4862 1655-1657 GeneOrGeneProduct denotes FH NCBIGene:2271
4863 1723-1736 DiseaseOrPhenotypicFeature denotes FH deficiency MESH:C538191
4864 1737-1745 OrganismTaxon denotes patients NCBITaxon:9606
4865 1750-1758 OrganismTaxon denotes patients NCBITaxon:9606
4866 1764-1768 DiseaseOrPhenotypicFeature denotes MCUL MESH:C535516
4867 1769-1774 DiseaseOrPhenotypicFeature denotes HLRRC MESH:C535516
4868 2052-2054 GeneOrGeneProduct denotes FH NCBIGene:2271
4869 2090-2092 GeneOrGeneProduct denotes FH NCBIGene:2271
4870 2176-2178 GeneOrGeneProduct denotes FH NCBIGene:2271
4871 2291-2299 OrganismTaxon denotes patients NCBITaxon:9606
4872 2447-2449 GeneOrGeneProduct denotes FH NCBIGene:2271