PubMed:16152606 JSONTXT 45 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
2226 30-37 SequenceVariant denotes 657del5 c|DEL|657|5
2227 45-49 GeneOrGeneProduct denotes NBS1 NCBIGene:4683
2228 91-99 OrganismTaxon denotes patients NCBITaxon:9606
2229 105-135 DiseaseOrPhenotypicFeature denotes sporadic lymphoid malignancies MESH:D008223
2230 137-163 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome MESH:D049932
2231 165-168 DiseaseOrPhenotypicFeature denotes NBS MESH:D049932
2232 175-180 OrganismTaxon denotes human NCBITaxon:9606
2233 181-208 DiseaseOrPhenotypicFeature denotes autosomal recessive disease MESH:D030342
2234 259-265 DiseaseOrPhenotypicFeature denotes cancer MESH:D009369
2235 299-307 DiseaseOrPhenotypicFeature denotes lymphoma MESH:D008223
2236 312-320 DiseaseOrPhenotypicFeature denotes leukemia MESH:D007938
2237 412-416 GeneOrGeneProduct denotes NBS1 NCBIGene:4683
2238 427-434 SequenceVariant denotes 657del5 c|DEL|657|5
2239 472-502 DiseaseOrPhenotypicFeature denotes sporadic lymphoid malignancies MESH:D008223
2240 530-550 DiseaseOrPhenotypicFeature denotes non-Hodgkin lymphoma MESH:D008228
2241 552-555 DiseaseOrPhenotypicFeature denotes NHL MESH:D008228
2242 588-594 SequenceVariant denotes 643C>T c|SUB|C|643|T
2243 596-601 SequenceVariant denotes R215W p|SUB|R|215|W
2244 653-681 DiseaseOrPhenotypicFeature denotes acute lymphoblastic leukemia MESH:D054198
2245 683-686 DiseaseOrPhenotypicFeature denotes ALL MESH:D054198
2246 769-799 DiseaseOrPhenotypicFeature denotes sporadic lymphoid malignancies MESH:D008223
2247 864-872 OrganismTaxon denotes patients NCBITaxon:9606
2248 878-882 GeneOrGeneProduct denotes NBS1 NCBIGene:4683
2249 892-899 SequenceVariant denotes 657del5 c|DEL|657|5
2250 936-944 OrganismTaxon denotes patients NCBITaxon:9606
2251 950-953 DiseaseOrPhenotypicFeature denotes ALL MESH:D054198
2252 997-1000 DiseaseOrPhenotypicFeature denotes NHL MESH:D008228
2253 1032-1040 OrganismTaxon denotes patients NCBITaxon:9606
2254 1046-1062 DiseaseOrPhenotypicFeature denotes Hodgkin lymphoma MESH:D006689
2255 1064-1066 DiseaseOrPhenotypicFeature denotes HL MESH:D006689
2256 1096-1101 SequenceVariant denotes R215W p|SUB|R|215|W
2257 1168-1175 SequenceVariant denotes 657del5 c|DEL|657|5
2258 1251-1258 OrganismTaxon denotes patient NCBITaxon:9606
2259 1360-1372 DiseaseOrPhenotypicFeature denotes malignancies MESH:D009369
2260 1429-1436 SequenceVariant denotes 657del5 c|DEL|657|5
2261 1644-1652 OrganismTaxon denotes patients NCBITaxon:9606
2262 1658-1661 DiseaseOrPhenotypicFeature denotes ALL MESH:D054198
2263 1666-1669 DiseaseOrPhenotypicFeature denotes NHL MESH:D008228
2264 1695-1699 GeneOrGeneProduct denotes NBS1 NCBIGene:4683
2265 1751-1772 DiseaseOrPhenotypicFeature denotes lymphoid malignancies MESH:D008223