PubMed:17910065 JSONTXT 34 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue db_id
4412 50-55 OrganismTaxon denotes human NCBITaxon:9606
4413 56-60 GeneOrGeneProduct denotes PAX9 NCBIGene:5083
4414 68-79 DiseaseOrPhenotypicFeature denotes oligodontia MESH:C538049
4415 81-85 GeneOrGeneProduct denotes PAX9 NCBIGene:5083
4416 90-94 GeneOrGeneProduct denotes MSX1 NCBIGene:4487
4417 188-194 OrganismTaxon denotes humans NCBITaxon:9606
4418 240-278 DiseaseOrPhenotypicFeature denotes nonsyndromic and syndromic oligodontia MESH:C538049
4419 322-346 DiseaseOrPhenotypicFeature denotes nonsyndromic oligodontia MESH:C538049
4420 364-368 GeneOrGeneProduct denotes PAX9 NCBIGene:5083
4421 373-377 GeneOrGeneProduct denotes MSX1 NCBIGene:4487
4422 484-489 SequenceVariant denotes C139T DBSNP:rs121917720
4423 504-508 GeneOrGeneProduct denotes PAX9 NCBIGene:5083
4424 614-618 GeneOrGeneProduct denotes MSX1 NCBIGene:4487
4425 624-629 SequenceVariant denotes C139T DBSNP:rs121917720
4426 686-710 SequenceVariant denotes arginine by a tryptophan DBSNP:rs121917720
4427 712-716 SequenceVariant denotes R47W DBSNP:rs121917720
4428 782-786 GeneOrGeneProduct denotes PAX9 NCBIGene:5083
4429 850-871 DiseaseOrPhenotypicFeature denotes oligodontia phenotype MESH:C538049
4430 945-949 GeneOrGeneProduct denotes PAX9 NCBIGene:5083
4431 1008-1012 SequenceVariant denotes R47W DBSNP:rs121917720