PubMed:23069675 JSONTXT 29 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
9140 17-37 GeneOrGeneProduct denotes neuronal pentraxin 1 NCBIGene:18164
9141 63-95 DiseaseOrPhenotypicFeature denotes hypoxic-ischemic neuronal injury MESH:D020925
9142 139-167 DiseaseOrPhenotypicFeature denotes hypoxic-ischemic (HI) injury MESH:D020925
9143 186-211 DiseaseOrPhenotypicFeature denotes neurological disabilities MESH:D009461
9144 289-309 GeneOrGeneProduct denotes neuronal pentraxin 1 NCBIGene:266777
9145 311-314 GeneOrGeneProduct denotes NP1 NCBIGene:266777
9146 378-396 DiseaseOrPhenotypicFeature denotes HI neuronal injury MESH:D020925
9147 472-489 DiseaseOrPhenotypicFeature denotes HI neuronal death MESH:D020925
9148 518-521 GeneOrGeneProduct denotes NP1 NCBIGene:18164
9149 532-535 GeneOrGeneProduct denotes NP1 NCBIGene:18164
9150 540-545 OrganismTaxon denotes mouse NCBITaxon:10090
9151 607-613 ChemicalEntity denotes oxygen MESH:D010100
9152 614-621 ChemicalEntity denotes glucose MESH:D005947
9153 670-675 OrganismTaxon denotes mouse NCBITaxon:10090
9154 685-700 DiseaseOrPhenotypicFeature denotes HI brain injury MESH:D020925
9155 732-735 GeneOrGeneProduct denotes NP1 NCBIGene:18164
9156 833-836 GeneOrGeneProduct denotes CA1 NCBIGene:12346
9157 841-844 GeneOrGeneProduct denotes CA3 NCBIGene:12350
9158 932-936 GeneOrGeneProduct denotes PTEN NCBIGene:19211
9159 1010-1013 GeneOrGeneProduct denotes Akt NCBIGene:11651
9160 1015-1021 SequenceVariant denotes Ser473 p|AellelS|473
9161 1027-1033 GeneOrGeneProduct denotes GSK-3β NCBIGene:56637
9162 1035-1039 SequenceVariant denotes Ser9 p|AellelS|9
9163 1110-1113 GeneOrGeneProduct denotes Bad NCBIGene:12015
9164 1115-1121 SequenceVariant denotes Ser136 p|AellelS|136
9165 1128-1131 GeneOrGeneProduct denotes Bax NCBIGene:12028
9166 1265-1268 GeneOrGeneProduct denotes Bad NCBIGene:12015
9167 1273-1276 GeneOrGeneProduct denotes Bax NCBIGene:12028
9168 1361-1366 GeneOrGeneProduct denotes Cyt C NCBIGene:13063
9169 1411-1420 GeneOrGeneProduct denotes caspase-3 NCBIGene:12367
9170 1422-1425 GeneOrGeneProduct denotes NP1 NCBIGene:18164
9171 1462-1465 GeneOrGeneProduct denotes Bad NCBIGene:12015
9172 1470-1473 GeneOrGeneProduct denotes Bax NCBIGene:12028
9173 1521-1524 GeneOrGeneProduct denotes NP1 NCBIGene:18164
9174 1530-1533 GeneOrGeneProduct denotes Bad NCBIGene:12015
9175 1538-1541 GeneOrGeneProduct denotes Bax NCBIGene:12028
9176 1665-1668 GeneOrGeneProduct denotes NP1 NCBIGene:18164
9177 1727-1739 GeneOrGeneProduct denotes cytochrome C NCBIGene:13063
9178 1741-1746 GeneOrGeneProduct denotes Cyt C NCBIGene:13063
9179 1780-1789 GeneOrGeneProduct denotes caspase-3 NCBIGene:12367
9180 1875-1878 GeneOrGeneProduct denotes NP1 NCBIGene:18164
9181 1920-1923 GeneOrGeneProduct denotes Bad NCBIGene:12015
9182 1928-1931 GeneOrGeneProduct denotes Bax NCBIGene:12028
9183 2007-2012 GeneOrGeneProduct denotes Cyt C NCBIGene:13063
9184 2025-2034 GeneOrGeneProduct denotes caspase-3 NCBIGene:12367
9185 2101-2115 DiseaseOrPhenotypicFeature denotes neuronal death MESH:D009410
9186 2159-2162 GeneOrGeneProduct denotes NP1 NCBIGene:18164
9187 2166-2169 GeneOrGeneProduct denotes Bad NCBIGene:12015
9188 2170-2173 GeneOrGeneProduct denotes Bax NCBIGene:12028
9189 2209-2214 GeneOrGeneProduct denotes Cyt C NCBIGene:13063
9190 2219-2228 GeneOrGeneProduct denotes caspase-3 NCBIGene:12367
9191 2302-2305 GeneOrGeneProduct denotes NP1 NCBIGene:18164
9192 2371-2374 GeneOrGeneProduct denotes NP1 NCBIGene:18164
9193 2417-2432 DiseaseOrPhenotypicFeature denotes HI brain injury MESH:D020925