PubMed:16158428 JSONTXT 25 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function

Id Subject Object Predicate Lexical cue db_id
2292 54-59 GeneOrGeneProduct denotes OPHN1 NCBIGene:4983
2293 200-205 GeneOrGeneProduct denotes OPHN1 NCBIGene:4983
2294 269-287 DiseaseOrPhenotypicFeature denotes mental retardation MESH:D008607
2295 331-352 DiseaseOrPhenotypicFeature denotes cerebellar hypoplasia MESH:C562568
2296 388-396 OrganismTaxon denotes patients NCBITaxon:9606
2297 448-475 DiseaseOrPhenotypicFeature denotes X-linked mental retardation MESH:D038901
2298 495-500 GeneOrGeneProduct denotes OPHN1 NCBIGene:4983
2299 683-704 DiseaseOrPhenotypicFeature denotes cerebellar hypoplasia MESH:C562568
2300 853-871 DiseaseOrPhenotypicFeature denotes mental retardation MESH:D008607