PubMed:19276632 JSONTXT 27 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue db_id
5820 21-26 GeneOrGeneProduct denotes FOXF2 NCBIGene:2295
5821 30-38 OrganismTaxon denotes patients NCBITaxon:9606
5822 44-72 DiseaseOrPhenotypicFeature denotes disorders of sex development MESH:D012734
5823 74-77 DiseaseOrPhenotypicFeature denotes DSD MESH:D012734
5824 99-111 DiseaseOrPhenotypicFeature denotes cleft palate MESH:D002972
5825 128-163 DiseaseOrPhenotypicFeature denotes disorders of sexual differentiation MESH:D012734
5826 182-190 ChemicalEntity denotes androgen MESH:D000728
5827 215-223 ChemicalEntity denotes androgen MESH:D000728
5828 327-333 OrganismTaxon denotes humans NCBITaxon:9606
5829 395-400 GeneOrGeneProduct denotes FOXF2 NCBIGene:2295
5830 424-429 OrganismTaxon denotes human NCBITaxon:9606
5831 450-455 GeneOrGeneProduct denotes Foxf2 NCBIGene:14238
5832 465-469 OrganismTaxon denotes mice NCBITaxon:10090
5833 483-495 DiseaseOrPhenotypicFeature denotes cleft palate MESH:D002972
5834 516-550 DiseaseOrPhenotypicFeature denotes hypoplasia of the genital tubercle MESH:C537540
5835 573-579 OrganismTaxon denotes humans NCBITaxon:9606
5836 585-613 DiseaseOrPhenotypicFeature denotes disorders of sex development MESH:D012734
5837 615-618 DiseaseOrPhenotypicFeature denotes DSD MESH:D012734
5838 640-652 DiseaseOrPhenotypicFeature denotes cleft palate MESH:D002972
5839 681-686 GeneOrGeneProduct denotes FOXF2 NCBIGene:2295
5840 716-719 DiseaseOrPhenotypicFeature denotes DSD MESH:D012734
5841 724-736 DiseaseOrPhenotypicFeature denotes cleft palate MESH:D002972
5842 767-770 DiseaseOrPhenotypicFeature denotes DSD MESH:D012734
5843 840-845 GeneOrGeneProduct denotes FOXF2 NCBIGene:2295
5844 1018-1025 OrganismTaxon denotes patient NCBITaxon:9606
5845 1072-1090 SequenceVariant denotes duplication of GCC c|DUP||GCC|
5846 1092-1107 SequenceVariant denotes c.97GCC[9]+[10] c|DUP|97|GCC|9-10
5847 1159-1165 SequenceVariant denotes 25*G>A c|SUB|G|*25|A
5848 1214-1222 OrganismTaxon denotes patients NCBITaxon:9606
5849 1233-1241 SequenceVariant denotes c.262G>A DBSNP:rs72667003
5850 1279-1287 SequenceVariant denotes Ala88Thr DBSNP:rs72667003
5851 1365-1374 SequenceVariant denotes c.1272C>T DBSNP:rs61753348
5852 1376-1385 SequenceVariant denotes Ser424Ser DBSNP:rs61753348
5853 1391-1400 SequenceVariant denotes c.1284T>C DBSNP:rs2293783
5854 1402-1411 SequenceVariant denotes Tyr428Tyr DBSNP:rs2293783
5855 1483-1491 OrganismTaxon denotes patients NCBITaxon:9606
5856 1729-1734 GeneOrGeneProduct denotes FOXF2 NCBIGene:2295