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sonoma

Id Subject Object Predicate Lexical cue
T-0 14-20 GENE denotes Hoxc13
T-1 21-29 VAR denotes knockout
T-2 35-48 REG denotes recapitulates
T-3 55-77 DISEASE denotes ectodermal dysplasia-9
T-4 79-87 DISEASE denotes Atrichia
T-5 92-113 CPA denotes sparse hair phenotype
T-6 114-119 REG denotes cause
T-7 147-169 DISEASE denotes Ectodermal dysplasia-9
T-8 171-175 DISEASE denotes ED-9
T-9 203-216 REG denotes characterized
T-10 282-288 GENE denotes Hoxc13
T-11 294-304 REG denotes pathogenic
T-12 314-318 DISEASE denotes ED-9
T-13 343-349 GENE denotes Hoxc13
T-14 350-358 VAR denotes mutation
T-15 359-366 REG denotes present
T-16 408-424 CPA denotes skeletal defects
T-17 426-449 CPA denotes progressive weight loss
T-18 454-457 NEGREG denotes low
T-19 458-467 CPA denotes viability
T-20 500-505 REG denotes mimic
T-21 512-516 DISEASE denotes ED-9
T-22 549-553 DISEASE denotes ED-9
T-23 568-574 GENE denotes Hoxc13
T-24 580-588 VAR denotes knockout
T-25 631-637 VAR denotes c.396C
T-27 755-764 VAR denotes mutations
T-28 799-807 VAR denotes A/c.396C
T-30 845-861 VAR denotes A/c.396C > A + 1
T-31 912-918 GENE denotes Hoxc13
T-32 923-926 NEGREG denotes not
T-33 927-936 MPA denotes expressed
T-34 960-968 VAR denotes mutation
T-35 984-994 MPA denotes expression
T-36 1005-1021 GENE denotes Hoxc13-regulated
T-37 1037-1042 GENE denotes Foxn1
T-38 1044-1049 GENE denotes Krt85
T-39 1054-1059 GENE denotes Krt35
T-40 1066-1075 NEGREG denotes decreased
T-41 1081-1095 CPA denotes hair follicles
T-42 1096-1105 REG denotes displayed
T-43 1114-1122 NEGREG denotes abnormal
T-44 1123-1133 CPA denotes phenotypes
T-45 1143-1150 NEGREG denotes reduced
T-46 1175-1185 NEGREG denotes disarrayed
T-47 1262-1276 CPA denotes skin structure
T-48 1278-1296 CPA denotes skeleton phenotype
T-49 1298-1314 CPA denotes body weight gain
T-50 1319-1325 CPA denotes growth
T-51 1329-1335 GENE denotes Hoxc13
T-52 1336-1344 VAR denotes knockout
T-53 1366-1372 NEGREG denotes normal
T-54 1378-1388 CPA denotes phenotypes
T-55 1392-1398 GENE denotes Hoxc13
T-56 1399-1407 VAR denotes mutation
T-57 1421-1428 REG denotes similar
T-58 1441-1445 DISEASE denotes ED-9
T-59 1467-1473 GENE denotes Hoxc13
T-60 1474-1482 VAR denotes knockout
T-61 1521-1525 DISEASE denotes ED-9
T-62 1548-1556 CPA denotes hairless
T-63 1567-1584 CPA denotes hair regeneration
T-64 1609-1617 CPA denotes hairless
R-0 T-0 T-1 ThemeOf Hoxc13,knockout
R-1 T-1 T-2 CauseOf knockout,recapitulates
R-2 T-3 T-2 ThemeOf ectodermal dysplasia-9,recapitulates
R-3 T-4 T-6 ThemeOf Atrichia,cause
R-4 T-5 T-6 ThemeOf sparse hair phenotype,cause
R-11 T-12 T-11 ThemeOf ED-9,pathogenic
R-12 T-13 T-14 ThemeOf Hoxc13,mutation
R-13 T-14 T-15 CauseOf mutation,present
R-14 T-14 T-18 CauseOf mutation,low
R-15 T-16 T-15 ThemeOf skeletal defects,present
R-16 T-17 T-15 ThemeOf progressive weight loss,present
R-17 T-18 T-15 ThemeOf low,present
R-18 T-19 T-15 ThemeOf viability,present
R-19 T-19 T-18 ThemeOf viability,low
R-20 T-21 T-20 ThemeOf ED-9,mimic
R-21 T-23 T-24 ThemeOf Hoxc13,knockout
R-22 T-23 T-25 ThemeOf Hoxc13,c.396C
R-50 T-55 T-56 ThemeOf Hoxc13,mutation
R-51 T-56 T-57 CauseOf mutation,similar
R-52 T-58 T-57 ThemeOf ED-9,similar
R-53 T-59 T-60 ThemeOf Hoxc13,knockout
R-5 T-7 T-9 ThemeOf Ectodermal dysplasia-9,characterized
R-6 T-7 T-11 ThemeOf Ectodermal dysplasia-9,pathogenic
R-7 T-8 T-9 ThemeOf ED-9,characterized
R-8 T-8 T-11 ThemeOf ED-9,pathogenic
R-9 T-10 T-11 ThemeOf Hoxc13,pathogenic
R-10 T-12 T-9 ThemeOf ED-9,characterized
R-24 T-31 T-32 ThemeOf Hoxc13,not
R-25 T-31 T-33 ThemeOf Hoxc13,expressed
R-26 T-31 T-34 ThemeOf Hoxc13,mutation
R-27 T-33 T-32 ThemeOf expressed,not
R-28 T-34 T-32 CauseOf mutation,not
R-29 T-34 T-40 CauseOf mutation,decreased
R-30 T-36 T-35 ThemeOf Hoxc13-regulated,expression
R-31 T-35 T-40 ThemeOf expression,decreased
R-32 T-37 T-34 ThemeOf Foxn1,mutation
R-33 T-37 T-35 ThemeOf Foxn1,expression
R-34 T-37 T-40 ThemeOf Foxn1,decreased
R-35 T-38 T-34 ThemeOf Krt85,mutation
R-36 T-38 T-35 ThemeOf Krt85,expression
R-37 T-38 T-40 ThemeOf Krt85,decreased
R-38 T-39 T-34 ThemeOf Krt35,mutation
R-39 T-39 T-35 ThemeOf Krt35,expression
R-40 T-41 T-42 ThemeOf hair follicles,displayed
R-41 T-41 T-43 ThemeOf hair follicles,abnormal
R-42 T-43 T-42 ThemeOf abnormal,displayed
R-43 T-44 T-43 ThemeOf phenotypes,abnormal
R-44 T-44 T-42 ThemeOf phenotypes,displayed
R-45 T-44 T-45 ThemeOf phenotypes,reduced
R-46 T-51 T-52 ThemeOf Hoxc13,knockout
R-47 T-52 T-53 CauseOf knockout,normal
R-48 T-56 T-54 CauseOf mutation,phenotypes
R-49 T-55 T-54 ThemeOf Hoxc13,phenotypes

sonoma2

Id Subject Object Predicate Lexical cue
T82 1567-1584 CPA denotes hair regeneration
T83 1643-1662 CPA denotes abnormal phenotypes
T0 14-20 GENE denotes Hoxc13
T1 21-29 VAR denotes knockout
T2 55-77 DISEASE denotes ectodermal dysplasia-9
T3 66-77 DISEASE denotes dysplasia-9
T4 79-87 DISEASE denotes Atrichia
T5 79-103 DISEASE denotes Atrichia and sparse hair
T6 92-113 CPA denotes sparse hair phenotype
T7 120-128 MPA denotes distress
T8 147-169 DISEASE denotes Ectodermal dysplasia-9
T9 171-175 DISEASE denotes ED-9
T10 203-216 REG denotes characterized
T11 220-233 DISEASE denotes hypotrichosis
T12 238-252 CPA denotes nail dystrophy
T13 238-252 DISEASE denotes nail dystrophy
T14 267-276 CPA denotes disorders
T15 282-288 GENE denotes Hoxc13
T16 294-304 NEGREG denotes pathogenic
T17 314-318 DISEASE denotes ED-9
T18 343-349 GENE denotes Hoxc13
T19 350-358 VAR denotes mutation
T20 359-366 REG denotes present
T21 381-398 CPA denotes serious disorders
T22 408-424 DISEASE denotes skeletal defects
T23 417-424 CPA denotes defects
T24 426-449 CPA denotes progressive weight loss
T25 438-449 DISEASE denotes weight loss
T26 454-457 NEGREG denotes low
T27 458-467 CPA denotes viability
T28 512-516 DISEASE denotes ED-9
T29 549-553 DISEASE denotes ED-9
T30 568-574 GENE denotes Hoxc13
T31 580-588 VAR denotes knockout
T32 597-629 VAR denotes single-stranded oligonucleotides
T33 631-641 VAR denotes c.396C > A
T34 657-668 VAR denotes CRISPR/Cas9
T35 745-764 VAR denotes biallelic mutations
T36 784-796 VAR denotes Hoxc13c.396C
T37 799-807 VAR denotes A/c.396C
T38 830-842 VAR denotes Hoxc13c.396C
T39 845-853 VAR denotes A/c.396C
T40 854-859 VAR denotes > A +
T41 882-895 VAR denotes Hoxc13Δ40/Δ40
T42 912-918 GENE denotes Hoxc13
T43 923-926 NEGREG denotes not
T44 927-936 MPA denotes expressed
T45 935-941 GENE denotes d in p
T46 960-968 VAR denotes mutation
T47 984-994 MPA denotes expression
T48 1022-1027 GENE denotes genes
T49 1028-1044 GENE denotes namely, Foxn1,
T50 1037-1042 GENE denotes Foxn1
T51 1044-1049 GENE denotes Krt85
T52 1054-1059 GENE denotes Krt35
T53 1060-1065 GENE denotes were
T54 1066-1075 NEGREG denotes decreased
T55 1067-1072 GENE denotes ecrea
T56 1077-1082 GENE denotes The h
T57 1081-1095 CPA denotes hair follicles
T58 1096-1105 REG denotes displayed
T59 1123-1133 CPA denotes phenotypes
T60 1143-1150 NEGREG denotes reduced
T61 1151-1170 CPA denotes number of follicles
T62 1175-1185 NEGREG denotes disarrayed
T63 1186-1205 CPA denotes hair follicle cable
T64 1221-1225 CPA denotes hair
T65 1262-1276 CPA denotes skin structure
T66 1278-1296 CPA denotes skeleton phenotype
T67 1298-1314 CPA denotes body weight gain
T68 1319-1325 CPA denotes growth
T69 1326-1337 DISEASE denotes of Hoxc13 k
T70 1329-1335 GENE denotes Hoxc13
T71 1336-1344 VAR denotes knockout
T72 1352-1358 GENE denotes re app
T73 1378-1388 CPA denotes phenotypes
T74 1392-1398 GENE denotes Hoxc13
T75 1399-1407 VAR denotes mutation
T76 1415-1421 GENE denotes were
T77 1441-1445 DISEASE denotes ED-9
T78 1467-1473 GENE denotes Hoxc13
T79 1474-1482 VAR denotes knockout
T80 1490-1496 GENE denotes uld be
T81 1521-1525 DISEASE denotes ED-9
R0 T0 T1 ThemeOf Hoxc13,knockout
R1 T4 T7 ThemeOf Atrichia,distress
R2 T8 T10 ThemeOf Ectodermal dysplasia-9,characterized
R3 T9 T10 ThemeOf ED-9,characterized
R4 T11 T10 ThemeOf hypotrichosis,characterized
R5 T11 T14 ThemeOf hypotrichosis,disorders
R6 T11 T16 ThemeOf hypotrichosis,pathogenic
R7 T12 T10 ThemeOf nail dystrophy,characterized
R8 T12 T14 ThemeOf nail dystrophy,disorders
R9 T14 T10 ThemeOf disorders,characterized
R10 T14 T16 ThemeOf disorders,pathogenic
R11 T17 T10 ThemeOf ED-9,characterized
R12 T17 T16 ThemeOf ED-9,pathogenic
R13 T18 T19 ThemeOf Hoxc13,mutation
R14 T19 T20 CauseOf mutation,present
R15 T19 T21 CauseOf mutation,serious disorders
R16 T19 T23 CauseOf mutation,defects
R17 T19 T24 CauseOf mutation,progressive weight loss
R18 T19 T26 CauseOf mutation,low
R19 T21 T20 ThemeOf serious disorders,present
R20 T23 T21 ThemeOf defects,serious disorders
R21 T24 T21 ThemeOf progressive weight loss,serious disorders
R22 T21 T26 ThemeOf serious disorders,low
R23 T23 T20 ThemeOf defects,present
R24 T24 T20 ThemeOf progressive weight loss,present
R25 T27 T21 ThemeOf viability,serious disorders
R26 T27 T26 ThemeOf viability,low
R27 T31 T29 CauseOf knockout,ED-9
R28 T32 T29 CauseOf single-stranded oligonucleotides,ED-9
R29 T30 T31 ThemeOf Hoxc13,knockout
R30 T30 T32 ThemeOf Hoxc13,single-stranded oligonucleotides
R31 T30 T33 ThemeOf Hoxc13,c.396C > A
R32 T30 T34 ThemeOf Hoxc13,CRISPR/Cas9
R33 T32 T31 CauseOf single-stranded oligonucleotides,knockout
R34 T33 T29 CauseOf c.396C > A,ED-9
R35 T34 T31 ThemeOf CRISPR/Cas9,knockout
R36 T34 T32 ThemeOf CRISPR/Cas9,single-stranded oligonucleotides
R37 T37 T36 ThemeOf A/c.396C,Hoxc13c.396C
R38 T39 T38 ThemeOf A/c.396C,Hoxc13c.396C
R39 T40 T38 ThemeOf > A +,Hoxc13c.396C
R40 T39 T40 ThemeOf A/c.396C,> A +
R41 T41 T35 ThemeOf Hoxc13Δ40/Δ40,biallelic mutations
R42 T42 T44 ThemeOf Hoxc13,expressed
R43 T42 T46 ThemeOf Hoxc13,mutation
R44 T42 T47 ThemeOf Hoxc13,expression
R45 T44 T43 ThemeOf expressed,not
R46 T44 T46 ThemeOf expressed,mutation
R47 T44 T54 ThemeOf expressed,decreased
R48 T46 T43 CauseOf mutation,not
R49 T46 T54 CauseOf mutation,decreased
R50 T47 T54 ThemeOf expression,decreased
R51 T48 T46 ThemeOf genes,mutation
R52 T48 T47 ThemeOf genes,expression
R53 T48 T54 ThemeOf genes,decreased
R54 T50 T46 ThemeOf Foxn1,mutation
R55 T50 T47 ThemeOf Foxn1,expression
R56 T51 T46 ThemeOf Krt85,mutation
R57 T51 T47 ThemeOf Krt85,expression
R58 T52 T46 ThemeOf Krt35,mutation
R59 T52 T47 ThemeOf Krt35,expression
R60 T57 T58 ThemeOf hair follicles,displayed
R61 T57 T59 ThemeOf hair follicles,phenotypes
R62 T59 T58 ThemeOf phenotypes,displayed
R63 T59 T60 ThemeOf phenotypes,reduced
R64 T61 T58 ThemeOf number of follicles,displayed
R65 T61 T59 ThemeOf number of follicles,phenotypes
R66 T61 T60 ThemeOf number of follicles,reduced
R67 T63 T58 ThemeOf hair follicle cable,displayed
R68 T63 T62 ThemeOf hair follicle cable,disarrayed
R69 T64 T58 ThemeOf hair,displayed
R70 T71 T68 CauseOf knockout,growth
R71 T70 T71 ThemeOf Hoxc13,knockout
R72 T74 T75 ThemeOf Hoxc13,mutation
R73 T75 T73 CauseOf mutation,phenotypes
R74 T78 T79 ThemeOf Hoxc13,knockout