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PubMed:19246455 JSONTXT 26 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 4-12 Species:7091 denotes silkworm
T2 20-25 Species:2708 denotes lemon
T3 27-32 Species:2708 denotes lemon
T4 73-78 Species:9606 denotes human
T5 91-111 Disease:MESH:C536415 denotes reductase deficiency
T6 113-132 Chemical:MESH:C003402 denotes Tetrahydrobiopterin
T7 134-137 Chemical:MESH:C003402 denotes BH4
T8 224-233 Chemical:- denotes monoamine
T9 253-256 Chemical:MESH:C003402 denotes BH4
T10 331-347 Disease:MESH:D030342 denotes inherited defect
T11 351-354 Chemical:MESH:C003402 denotes BH4
T12 385-420 Disease:MESH:C562657 denotes deficiency of sepiapterin reductase
T13 422-425 Gene:6697 denotes SPR
T14 464-467 Chemical:MESH:C003402 denotes BH4
T15 473-495 Chemical:MESH:D006160 denotes guanosine triphosphate
T16 522-527 Species:9606 denotes human
T17 528-531 Gene:6697 denotes SPR
T18 560-565 Gene:5072 denotes PARK3
T19 606-623 Disease:MESH:D010300 denotes Parkinson disease
T20 671-676 Species:2708 denotes lemon
T21 678-681 Species:2708 denotes lem
T22 705-710 Species:2708 denotes lemon
T23 719-722 Species:2708 denotes lem
T24 763-771 Species:7091 denotes silkworm
T25 772-783 Species:7091 denotes Bombyx mori
T26 828-833 Species:9606 denotes human
T27 834-837 Gene:6697 denotes SPR
T28 838-857 Disease:MESH:D030342 denotes deficiency diseases
T29 897-900 Gene:6697 denotes SPR
T30 907-912 Gene:100379197 denotes BmSpr
T31 968-971 Species:2708 denotes lem
T32 976-979 Species:2708 denotes lem
T33 1029-1032 Gene:6697 denotes SPR
T34 1045-1048 Species:2708 denotes lem
T35 1226-1229 Chemical:MESH:C003402 denotes BH4
T36 1234-1242 Chemical:MESH:D004298 denotes dopamine
T37 1246-1249 Species:2708 denotes lem
T38 1352-1357 Gene:100379197 denotes BmSPR
T39 1400-1403 Chemical:MESH:C003402 denotes BH4
T40 1409-1418 Chemical:- denotes monoamine
T41 1440-1449 Species:7091 denotes silkworms
T42 1458-1461 Species:2708 denotes lem
T43 1463-1466 Species:2708 denotes lem
T44 1553-1556 Gene:6697 denotes SPR
T45 1561-1577 Disease:MESH:D010661 denotes BH4 deficiencies