PubMed:27840894 JSONTXT 43 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
11675 28-32 GeneOrGeneProduct denotes PHEX NCBIGene:5251
11676 51-59 OrganismTaxon denotes patients NCBITaxon:9606
11677 65-89 DiseaseOrPhenotypicFeature denotes hypophosphatemic rickets MESH:D063730
11678 117-195 GeneOrGeneProduct denotes phosphate-regulating gene with homologies to endopeptidase on the X chromosome NCBIGene:5251
11679 197-201 GeneOrGeneProduct denotes PHEX NCBIGene:5251
11680 238-271 DiseaseOrPhenotypicFeature denotes X-linked hypophosphatemic rickets MESH:D053098
11681 273-276 DiseaseOrPhenotypicFeature denotes XLH MESH:D053098
11682 278-289 DiseaseOrPhenotypicFeature denotes OMIM 307800 MESH:D053098
11683 329-337 OrganismTaxon denotes patients NCBITaxon:9606
11684 391-415 DiseaseOrPhenotypicFeature denotes hypophosphatemic rickets MESH:D063730
11685 527-531 GeneOrGeneProduct denotes PHEX NCBIGene:5251
11686 582-609 GeneOrGeneProduct denotes fibroblast growth factor 23 NCBIGene:8074
11687 611-616 GeneOrGeneProduct denotes FGF23 NCBIGene:8074
11688 683-687 GeneOrGeneProduct denotes PHEX NCBIGene:5251
11689 777-785 SequenceVariant denotes c.304G>A c|SUB|G|304|A
11690 787-798 SequenceVariant denotes p.Gly102Arg p|SUB|G|102|R
11691 811-819 SequenceVariant denotes c.229T>C c|SUB|T|229|C
11692 821-831 SequenceVariant denotes p.Cys77Arg p|SUB|C|77|R
11693 847-855 SequenceVariant denotes c.824T>C c|SUB|T|284|C
11694 857-868 SequenceVariant denotes p.Leu275Pro p|SUB|L|275|P
11695 913-922 SequenceVariant denotes c.528delT c|DEL|528|T
11696 924-940 SequenceVariant denotes p.Glu177LysfsX44 p|SUB|E|177|K|44
11697 956-966 SequenceVariant denotes c.1234delA c|DEL|1234|A
11698 968-984 SequenceVariant denotes p.Ser412ValfsX12 p|SUB|S|412|V|12
11699 1046-1062 SequenceVariant denotes c.436_436+1delAG c|DEL|436_436+1|AG
11700 1103-1114 SequenceVariant denotes c.1483-1G>C c|SUB|G|1483-1|C
11701 1332-1337 GeneOrGeneProduct denotes FGF23 NCBIGene:8074
11702 1362-1370 OrganismTaxon denotes patients NCBITaxon:9606
11703 1376-1379 DiseaseOrPhenotypicFeature denotes XLH MESH:D053098
11704 1553-1557 GeneOrGeneProduct denotes PHEX NCBIGene:5251
11705 1623-1627 GeneOrGeneProduct denotes PHEX NCBIGene:5251
11706 1689-1694 GeneOrGeneProduct denotes FGF23 NCBIGene:8074
11707 1714-1722 OrganismTaxon denotes patients NCBITaxon:9606
11708 1728-1731 DiseaseOrPhenotypicFeature denotes XLH MESH:D053098
11709 1799-1802 DiseaseOrPhenotypicFeature denotes XLH MESH:D053098