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PubMed:24946076 JSONTXT 32 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T0 0-4 GENE denotes PDGF
T1 40-78 DISEASE denotes idiopathic basal ganglia calcification
T2 80-84 DISEASE denotes IBGC
T3 80-84 GENE denotes IBGC
T4 87-103 GENE denotes Platelet-derived
T5 310-319 POSREG denotes Increased
T6 331-335 GENE denotes PDGF
T7 336-344 MPA denotes activity
T8 354-359 REG denotes cause
T9 363-373 REG denotes contribute
T10 377-385 DISEASE denotes diseases
T11 394-400 DISEASE denotes cancer
T12 412-420 DISEASE denotes fibrosis
T13 441-457 NEGREG denotes loss-of-function
T14 459-462 NEGREG denotes LOF
T15 464-473 VAR denotes mutations
T16 477-481 GENE denotes PDGF
T17 485-489 GENE denotes PDGF
T18 531-537 REG denotes linked
T19 613-616 NEGREG denotes LOF
T20 617-626 VAR denotes mutations
T21 649-655 GENE denotes PDGF-B
T22 673-677 GENE denotes PDGF
T23 693-700 GENE denotes PDGF-Rβ
T24 693-703 GENE denotes PDGF-Rβ) i
T25 705-752 DISEASE denotes familial idiopathic basal ganglia calcification
T26 708-755 DISEASE denotes ilial idiopathic basal ganglia calcification (I
T27 754-758 DISEASE denotes IBGC
T28 757-761 GENE denotes C),
T29 766-779 DISEASE denotes in disease ch
T30 883-889 GENE denotes PDGF-B
T31 886-892 GENE denotes F-B an
T32 894-901 GENE denotes PDGF-Rβ
T33 897-907 GENE denotes F-Rβ biolo
T34 987-1007 CPA denotes pericyte recruitment
T35 1099-1103 GENE denotes atho
R0 T5 T8 CauseOf Increased,cause
R1 T6 T7 ThemeOf PDGF,activity
R10 T15 T18 CauseOf mutations,linked
R11 T16 T15 ThemeOf PDGF,mutations
R12 T17 T15 ThemeOf PDGF,mutations
R13 T20 T19 CauseOf mutations,LOF
R14 T21 T20 ThemeOf PDGF-B,mutations
R15 T22 T20 ThemeOf PDGF,mutations
R16 T23 T20 ThemeOf PDGF-Rβ,mutations
R17 T25 T19 ThemeOf familial idiopathic basal ganglia calcification,LOF
R18 T27 T19 ThemeOf IBGC,LOF
R2 T10 T9 ThemeOf diseases,contribute
R3 T11 T9 ThemeOf cancer,contribute
R4 T11 T10 ThemeOf cancer,diseases
R5 T12 T9 ThemeOf fibrosis,contribute
R6 T12 T10 ThemeOf fibrosis,diseases
R7 T14 T13 CauseOf LOF,loss-of-function
R8 T15 T13 CauseOf mutations,loss-of-function
R9 T15 T14 CauseOf mutations,LOF