PubMed:17221831 JSONTXT 28 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue db_id
3849 4-8 SequenceVariant denotes G51S DBSNP:rs1049564
3850 9-40 GeneOrGeneProduct denotes purine nucleoside phosphorylase NCBIGene:4860
3851 73-90 DiseaseOrPhenotypicFeature denotes cognitive decline MESH:D003072
3852 94-113 DiseaseOrPhenotypicFeature denotes Alzheimer's disease MESH:D000544
3853 114-122 OrganismTaxon denotes patients NCBITaxon:9606
3854 124-143 DiseaseOrPhenotypicFeature denotes Alzheimer's disease MESH:D000544
3855 145-147 DiseaseOrPhenotypicFeature denotes AD MESH:D000544
3856 522-534 DiseaseOrPhenotypicFeature denotes inflammatory MESH:D007249
3857 653-655 DiseaseOrPhenotypicFeature denotes AD MESH:D000544
3858 703-706 SequenceVariant denotes G/A DBSNP:rs1049564
3859 747-778 GeneOrGeneProduct denotes purine nucleoside phosphorylase NCBIGene:4860
3860 780-783 GeneOrGeneProduct denotes PNP NCBIGene:4860
3861 832-864 SequenceVariant denotes serine to glycine at position 51 DBSNP:rs1049564
3862 866-870 SequenceVariant denotes G51S DBSNP:rs1049564
3863 915-917 DiseaseOrPhenotypicFeature denotes AD MESH:D000544
3864 918-926 OrganismTaxon denotes patients NCBITaxon:9606
3865 973-976 GeneOrGeneProduct denotes PNP NCBIGene:4860
3866 1029-1037 OrganismTaxon denotes patients NCBITaxon:9606
3867 1103-1105 DiseaseOrPhenotypicFeature denotes AD MESH:D000544
3868 1106-1114 OrganismTaxon denotes patients NCBITaxon:9606
3869 1172-1189 DiseaseOrPhenotypicFeature denotes cognitive decline MESH:D003072
3870 1252-1255 GeneOrGeneProduct denotes PNP NCBIGene:4860
3871 1284-1286 DiseaseOrPhenotypicFeature denotes AD MESH:D000544
3872 1287-1295 OrganismTaxon denotes patients NCBITaxon:9606
3873 1306-1329 DiseaseOrPhenotypicFeature denotes cognitive deterioration MESH:D003072
3874 1359-1367 OrganismTaxon denotes patients NCBITaxon:9606
3875 1428-1432 SequenceVariant denotes G51S DBSNP:rs1049564
3876 1433-1436 GeneOrGeneProduct denotes PNP NCBIGene:4860
3877 1486-1503 DiseaseOrPhenotypicFeature denotes cognitive decline MESH:D003072
3878 1507-1509 DiseaseOrPhenotypicFeature denotes AD MESH:D000544
3879 1510-1518 OrganismTaxon denotes patients NCBITaxon:9606
3880 1600-1626 DiseaseOrPhenotypicFeature denotes neurodegenerative disorder MESH:D019636