LitCoin-entities  

PubMed:16005363 JSONTXT 33 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
2045 26-30 GeneOrGeneProduct denotes WFS1 NCBIGene:7466
2046 41-54 SequenceVariant denotes AFF344-345ins p|INS|344_345|AFF
2047 68-76 OrganismTaxon denotes patients NCBITaxon:9606
2048 82-98 DiseaseOrPhenotypicFeature denotes Wolfram syndrome MESH:D014929
2049 100-116 DiseaseOrPhenotypicFeature denotes Wolfram syndrome MESH:D014929
2050 118-121 DiseaseOrPhenotypicFeature denotes WFS MESH:D014929
2051 129-157 DiseaseOrPhenotypicFeature denotes autosomal recessive disorder MESH:D030342
2052 187-204 DiseaseOrPhenotypicFeature denotes diabetes mellitus MESH:D003920
2053 218-231 DiseaseOrPhenotypicFeature denotes optic atrophy MESH:D009896
2054 233-255 DiseaseOrPhenotypicFeature denotes sensorineural deafness MESH:D006319
2055 260-278 DiseaseOrPhenotypicFeature denotes diabetes insipidus MESH:D003919
2056 315-340 DiseaseOrPhenotypicFeature denotes renal tract abnormalities MESH:D007674
2057 367-388 DiseaseOrPhenotypicFeature denotes psychiatric syndromes MESH:D001523
2058 390-394 GeneOrGeneProduct denotes WFS1 NCBIGene:7466
2059 471-474 DiseaseOrPhenotypicFeature denotes WFS MESH:D014929
2060 559-563 GeneOrGeneProduct denotes WFS1 NCBIGene:7466
2061 578-586 OrganismTaxon denotes patients NCBITaxon:9606
2062 622-647 SequenceVariant denotes nine nucleotide insertion c|INS||9
2063 649-662 SequenceVariant denotes AFF344-345ins p|INS|344_345|AFF
2064 691-699 OrganismTaxon denotes patients NCBITaxon:9606
2065 716-731 DiseaseOrPhenotypicFeature denotes hypopituitarism MESH:D007018
2066 764-767 DiseaseOrPhenotypicFeature denotes WFS MESH:D014929
2067 835-838 DiseaseOrPhenotypicFeature denotes WFS MESH:D014929
2068 905-908 DiseaseOrPhenotypicFeature denotes WFS MESH:D014929