PubMed:24632946 JSONTXT 56 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label ID:
T75708 39-45 OrganismTaxon denotes cloaca
T1674 59-66 GeneOrGeneProduct denotes catenin
T66265 84-107 DiseaseOrPhenotypicFeature denotes anorectal malformations D000071056
T40876 113-119 OrganismTaxon denotes cloaca
T2 201-211 GeneOrGeneProduct denotes urogenital
T44392 254-278 DiseaseOrPhenotypicFeature denotes congenital malformations DISEASE
T7978 288-311 DiseaseOrPhenotypicFeature denotes anorectal malformations D000071056
T78214 313-317 DiseaseOrPhenotypicFeature denotes ARMs D000071056
T79000 420-427 GeneOrGeneProduct denotes Catenin
T4 599-606 GeneOrGeneProduct denotes catenin
T5 688-695 GeneOrGeneProduct denotes catenin
T1 752-761 ChemicalEntity denotes tamoxifen http://purl.obolibrary.org/obo/CHEBI_41774|D013629
T6 811-818 GeneOrGeneProduct denotes catenin
T90754 921-932 DiseaseOrPhenotypicFeature denotes hypoplastic DISEASE
T7 1052-1059 GeneOrGeneProduct denotes catenin
T3 1227-1250 ChemicalEntity denotes differentiation markers D000943
T8 1260-1269 GeneOrGeneProduct denotes keratin 1
T9 1274-1283 GeneOrGeneProduct denotes filaggrin
T10 1330-1356 GeneOrGeneProduct denotes bone morphogenetic protein
T11 1358-1361 GeneOrGeneProduct denotes Bmp
T12 1378-1382 GeneOrGeneProduct denotes Bmp4
T13 1387-1391 GeneOrGeneProduct denotes Bmp7
T14 1459-1466 GeneOrGeneProduct denotes catenin
T15 1502-1506 GeneOrGeneProduct denotes Msx2
T16 1531-1538 GeneOrGeneProduct denotes Smad1/5
T17 1563-1566 GeneOrGeneProduct denotes Bmp
T18 1666-1678 GeneOrGeneProduct denotes Bmp receptor
T20 1715-1722 GeneOrGeneProduct denotes catenin
T21 1828-1835 GeneOrGeneProduct denotes catenin
T35060 1882-1885 DiseaseOrPhenotypicFeature denotes ARM DISEASE
T22 1906-1913 GeneOrGeneProduct denotes catenin
T23 1950-1953 GeneOrGeneProduct denotes Bmp
T24 2030-2037 GeneOrGeneProduct denotes catenin
T53676 2055-2058 DiseaseOrPhenotypicFeature denotes ARM DISEASE
T64018 2146-2151 OrganismTaxon denotes human
T99015 2152-2156 DiseaseOrPhenotypicFeature denotes ARMs D000071056