PubMed:17345627 JSONTXT 33 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue db_id
4050 19-23 GeneOrGeneProduct denotes BMP4 NCBIGene:652
4051 28-32 GeneOrGeneProduct denotes BMP5 NCBIGene:653
4052 49-77 DiseaseOrPhenotypicFeature denotes axial skeletal malformations MESH:D001848
4053 82-106 DiseaseOrPhenotypicFeature denotes heterotopic ossification MESH:D009999
4054 124-151 GeneOrGeneProduct denotes Bone morphogenetic proteins NCBIGene:649|NCBIGene:650|NCBIGene:652|NCBIGene:653
4055 153-157 GeneOrGeneProduct denotes BMPs NCBIGene:649|NCBIGene:650|NCBIGene:652|NCBIGene:653
4056 223-259 DiseaseOrPhenotypicFeature denotes ectopic cartilage and bone formation MESH:D001847|MESH:D002357
4057 296-324 GeneOrGeneProduct denotes bone morphogenetic protein 4 NCBIGene:652
4058 326-330 GeneOrGeneProduct denotes BMP4 NCBIGene:652
4059 357-365 OrganismTaxon denotes patients NCBITaxon:9606
4060 375-412 DiseaseOrPhenotypicFeature denotes fibrodysplasia ossificans progressiva MESH:D009221
4061 414-417 DiseaseOrPhenotypicFeature denotes FOP MESH:D009221
4062 442-486 DiseaseOrPhenotypicFeature denotes axial and appendicular skeletal malformation MESH:D001848
4063 503-527 DiseaseOrPhenotypicFeature denotes heterotopic ossification MESH:D009999
4064 563-591 GeneOrGeneProduct denotes bone morphogenetic protein 5 NCBIGene:653
4065 593-597 GeneOrGeneProduct denotes bmp5 NCBIGene:653
4066 635-639 GeneOrGeneProduct denotes BMP5 NCBIGene:653
4067 650-656 OrganismTaxon denotes murine NCBITaxon:10090
4068 657-675 DiseaseOrPhenotypicFeature denotes short ear syndrome MESH:D004427
4069 736-764 DiseaseOrPhenotypicFeature denotes axial skeletal malformations MESH:D001848
4070 818-823 OrganismTaxon denotes mouse NCBITaxon:10090
4071 828-831 DiseaseOrPhenotypicFeature denotes FOP MESH:D009221
4072 848-871 DiseaseOrPhenotypicFeature denotes malformed external ears MESH:D004426
4073 873-917 DiseaseOrPhenotypicFeature denotes multiple malformations of the axial skeleton MESH:D001848
4074 935-959 DiseaseOrPhenotypicFeature denotes heterotopic ossification MESH:D009999
4075 994-997 GeneOrGeneProduct denotes BMP NCBIGene:649|NCBIGene:650|NCBIGene:652|NCBIGene:653
4076 1153-1157 GeneOrGeneProduct denotes BMP4 NCBIGene:652
4077 1162-1166 GeneOrGeneProduct denotes BMP5 NCBIGene:653
4078 1205-1212 OrganismTaxon denotes patient NCBITaxon:9606
4079 1237-1241 GeneOrGeneProduct denotes BMP2 NCBIGene:650
4080 1312-1316 GeneOrGeneProduct denotes BMP4 NCBIGene:652
4081 1321-1325 GeneOrGeneProduct denotes BMP5 NCBIGene:653
4082 1363-1368 OrganismTaxon denotes human NCBITaxon:9606
4083 1369-1397 DiseaseOrPhenotypicFeature denotes axial skeletal abnormalities MESH:D001848
4084 1423-1428 OrganismTaxon denotes mouse NCBITaxon:10090
4085 1433-1436 DiseaseOrPhenotypicFeature denotes FOP MESH:D009221