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 |