Mercurial > repos > dlalgroup > pmids_to_pubtator_matrix
view examples/data/1b/clingen_data @ 2:ada4c7b3fc39 draft default tip
"planemo upload for repository https://github.com/dlal-group/simtext commit 63f67ee02be2eb4323a5ba5dcdd33d1fd0b7c24e"
author | dlalgroup |
---|---|
date | Thu, 08 Oct 2020 05:39:58 +0000 |
parents | 3f4adc85ba5d |
children |
line wrap: on
line source
"ID_gene" "GROUPING_disorder" "1" "CHD2" "complex neurodevelopmental disorder" "2" "EEF1A2" "complex neurodevelopmental disorder" "3" "GRIN1" "complex neurodevelopmental disorder" "4" "GRIN2A" "complex neurodevelopmental disorder" "5" "KCNB1" "complex neurodevelopmental disorder" "6" "MEF2C" "complex neurodevelopmental disorder" "7" "NRXN1" "complex neurodevelopmental disorder" "8" "PURA" "complex neurodevelopmental disorder" "9" "SCN2A" "complex neurodevelopmental disorder" "10" "SCN8A" "complex neurodevelopmental disorder" "11" "SHANK2" "complex neurodevelopmental disorder" "12" "SYNGAP1" "complex neurodevelopmental disorder" "13" "CC2D1A" "complex neurodevelopmental disorder" "14" "HOXA1" "complex neurodevelopmental disorder" "15" "IQSEC2" "complex neurodevelopmental disorder" "16" "NLGN4X" "complex neurodevelopmental disorder" "17" "SMC1A" "complex neurodevelopmental disorder" "18" "UPF3B" "complex neurodevelopmental disorder" "19" "WDR45" "complex neurodevelopmental disorder" "20" "ACTA2" "familial thoracic aortic aneurysm and aortic dissection" "21" "COL3A1" "familial thoracic aortic aneurysm and aortic dissection" "22" "FBN1" "familial thoracic aortic aneurysm and aortic dissection" "23" "LOX" "familial thoracic aortic aneurysm and aortic dissection" "24" "MYH11" "familial thoracic aortic aneurysm and aortic dissection" "25" "MYLK" "familial thoracic aortic aneurysm and aortic dissection" "26" "PRKG1" "familial thoracic aortic aneurysm and aortic dissection" "27" "SMAD3" "familial thoracic aortic aneurysm and aortic dissection" "28" "TGFB2" "familial thoracic aortic aneurysm and aortic dissection" "29" "TGFBR1" "familial thoracic aortic aneurysm and aortic dissection" "30" "TGFBR2" "familial thoracic aortic aneurysm and aortic dissection" "31" "ACTG1" "nonsyndromic genetic deafness" "32" "COCH" "nonsyndromic genetic deafness" "33" "EYA4" "nonsyndromic genetic deafness" "34" "GRHL2" "nonsyndromic genetic deafness" "35" "KCNQ4" "nonsyndromic genetic deafness" "36" "MYH14" "nonsyndromic genetic deafness" "37" "MYO6" "nonsyndromic genetic deafness" "38" "MYO7A" "nonsyndromic genetic deafness" "39" "POU4F3" "nonsyndromic genetic deafness" "40" "SLC17A8" "nonsyndromic genetic deafness" "41" "TECTA" "nonsyndromic genetic deafness" "42" "TMC1" "nonsyndromic genetic deafness" "43" "CABP2" "nonsyndromic genetic deafness" "44" "CDH23" "nonsyndromic genetic deafness" "45" "CIB2" "nonsyndromic genetic deafness" "46" "CLDN14" "nonsyndromic genetic deafness" "47" "ESPN" "nonsyndromic genetic deafness" "48" "ESRRB" "nonsyndromic genetic deafness" "49" "GIPC3" "nonsyndromic genetic deafness" "50" "GRXCR1" "nonsyndromic genetic deafness" "51" "ILDR1" "nonsyndromic genetic deafness" "52" "LHFPL5" "nonsyndromic genetic deafness" "53" "LOXHD1" "nonsyndromic genetic deafness" "54" "MARVELD2" "nonsyndromic genetic deafness" "55" "MYO15A" "nonsyndromic genetic deafness" "56" "MYO3A" "nonsyndromic genetic deafness" "57" "OTOA" "nonsyndromic genetic deafness" "58" "OTOG" "nonsyndromic genetic deafness" "59" "OTOGL" "nonsyndromic genetic deafness" "60" "PJVK" "nonsyndromic genetic deafness" "61" "RDX" "nonsyndromic genetic deafness" "62" "S1PR2" "nonsyndromic genetic deafness" "63" "STRC" "nonsyndromic genetic deafness" "64" "TMIE" "nonsyndromic genetic deafness" "65" "TMPRSS3" "nonsyndromic genetic deafness" "66" "TPRN" "nonsyndromic genetic deafness" "67" "POU3F4" "nonsyndromic genetic deafness" "68" "SMPX" "nonsyndromic genetic deafness" "69" "KRAS" "Noonan syndrome" "70" "LZTR1" "Noonan syndrome" "71" "NRAS" "Noonan syndrome" "72" "PTPN11" "Noonan syndrome" "73" "RAF1" "Noonan syndrome" "74" "RIT1" "Noonan syndrome" "75" "RRAS2" "Noonan syndrome" "76" "SOS1" "Noonan syndrome" "77" "ETHE1" "Leigh syndrome" "78" "LRPPRC" "Leigh syndrome" "79" "NDUFS1" "Leigh syndrome" "80" "NDUFS4" "Leigh syndrome" "81" "NDUFV1" "Leigh syndrome" "82" "SCO2" "Leigh syndrome" "83" "SLC19A3" "Leigh syndrome" "84" "SUCLA2" "Leigh syndrome" "85" "SURF1" "Leigh syndrome" "86" "TTC19" "Leigh syndrome" "87" "PDHA1" "Leigh syndrome" "88" "ACTC1" "hypertrophic cardiomyopathy" "89" "MYH7" "hypertrophic cardiomyopathy" "90" "MYL3" "hypertrophic cardiomyopathy" "91" "PRKAG2" "hypertrophic cardiomyopathy" "92" "TNNI3" "hypertrophic cardiomyopathy" "93" "TNNT2" "hypertrophic cardiomyopathy" "94" "TPM1" "hypertrophic cardiomyopathy" "95" "ALPK3" "hypertrophic cardiomyopathy"