view test/data/pmids_to_pubtator_matrix_output @ 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
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line source

"24(s)-hydroxycholesterol"	"ablim2"	"acap2"	"acetonitrile"	"adamts20"	"adamts7"	"ahi1"	"alzheimer's"	"amphetamine"	"ankrd11"	"arginine"	"asd"	"astigmatism"	"autism"	"autism spectrum disorder"	"behavioral abnormalities"	"brd4"	"breast cancer"	"brugada syndrome"	"c26h6orf106"	"c6orf106"	"cacna1c"	"cacna1h"	"cacna2d2"	"calcium"	"cancer"	"cancerous overgrowth"	"cardiac and neuronal channelopathies"	"cardiac lesions"	"cardiomyopathy"	"cas"	"ccl16"	"cd14"	"cd31"	"cd45"	"cd49d"	"cd73"	"cd90"	"cdc42bpa"	"cdh15"	"cdk13"	"cdkl5"	"chromosomal abnormalities"	"clonidine"	"cntnap2"	"cognitive"	"col24a1"	"col4a2"	"col5a1"	"col6a3"	"congenital anomalies"	"contactin-associated protein-like 2"	"cooh"	"corneal neuralgia"	"cornelia de lange syndrome"	"cpe"	"craniofacial dysmorphisms"	"crebbp"	"ctnna1"	"ctu2"	"cystatin c"	"d-cycloserine"	"ddx3x"	"deficiency perturbs early neuronal"	"degs"	"depdc7"	"depression"	"depressive disorder"	"developmental defects"	"developmental delay"	"developmental dendritic"	"developmental human disorders"	"diabetes"	"dip2c"	"dip2cdelta2bp"	"disability (id) syndrome"	"dnah11"	"dnah9"	"dnlz"	"dry excreta weight"	"dry matter"	"dysmorphic"	"ebf3"	"edta"	"ees"	"ehmt1"	"eno2"	"enolase 2"	"ep300"	"epha1"	"epha10"	"epilepsy"	"epileptic encephalopathies"	"epileptic encephalopathy"	"epileptic spasm"	"erythromelalgia and paroxysmal extreme pain disorder"	"fatigue syndrome"	"fcr"	"fgd5"	"flt4"	"fn1"	"forkhead box p2"	"foxp2"	"fracture"	"fyco1"	"gaba"	"gabbr2"	"gabra5"	"gabra6"	"gabre"	"gabrq"	"gabrr2"	"gallus gallus chromosome"	"gap43"	"gga1"	"gga2"	"gingivitis"	"glutamate"	"glycine"	"gnao1"	"gnb1"	"grid2ip"	"grin1"	"grin2a"	"grin2b"	"grin2c"	"grm4"	"growth hormone"	"gtf2h1"	"hace1"	"haploinsufficiency"	"hdac8"	"hippo"	"hippocampal sclerosis"	"histamine receptor h3"	"hivep2"	"hnav1.7"	"hsa-mir-3664"	"hspa7"	"hyperopia"	"hypoplastic left"	"icu-sepsis"	"igf-1"	"igf1"	"infected"	"inflammation"	"insulin-like growth factor 1"	"intellectual disability"	"itih3"	"kank1"	"kbg"	"kbg syndrome"	"kchip2"	"kcnd3"	"kcnh1"	"kcnma1"	"kif24"	"kit"	"kmt2d"	"ksr1"	"ksr2"	"kv4.3"	"lamb4"	"lats1"	"lman1"	"lrp2"	"madd"	"mccc1"	"mdd"	"mdm"	"mecp2"	"meis2"	"memantine"	"metabolic disorders"	"mfsd8"	"mir-218"	"mirp3"	"mllt1"	"movement disorders"	"mtch1"	"mtx1"	"myc"	"myh11"	"myo1e"	"myopia"	"nav 1.1"	"nav1.5"	"nav1.7"	"ndds"	"neonatal saliva"	"nestin"	"neurexin 1"	"neurod1"	"neurodevelopmental disorders"	"neurofilament heavy polypeptide"	"neuronal defects"	"neuronal developmental defects"	"neuronal disorders"	"neuropathic"	"neuropathic pain"	"neuropathy"	"neuropsychiatric disorders"	"nfh"	"nipbl"	"nitrogen"	"nlgn2"	"noonan syndrome"	"nr2f2"	"nsun7"	"ovarian cancer"	"pain"	"pain syndromes"	"pcdh19"	"pde3b"	"pediatric heart disease"	"peptides"	"pgn"	"phosphopeptides"	"plxnb2"	"pogz"	"polyacrylamide"	"polyneuropathy"	"pom121c"	"poteb"	"prednisone"	"pregnenolone sulfate"	"ptpn11"	"pulmonary stenosis"	"pura"	"pus7l"	"rad21"	"regressive autism"	"rpl13"	"rps6kl1"	"rubinstein-taybi syndrome"	"rxrb"	"saa1"	"saa2"	"sall1"	"sbno1"	"sca19"	"sclerosis"	"scn10a"	"scn1a"	"scn2a"	"scn5a"	"scn8a"	"scn9a"	"sdcbp2"	"sds"	"seizure"	"seizures"	"sepsis"	"serine"	"setbp1"	"sfn"	"shank2"	"short stature"	"slc2a1"	"slc8a2"	"slc9a3r1"	"slc9a6"	"slx4"	"smarcc1"	"smc1a"	"smc2"	"smc3"	"smith-magenis syndrome"	"sms"	"snap25"	"social deficits"	"sodium"	"speech disorder"	"speech disorders"	"spinocerebellar ataxia"	"spondyloepimetaphyseal dysplasia isidor"	"structural abnormalities"	"supt6h"	"supv3l1"	"syde1"	"synaptophysin"	"syncope"	"tachycardia"	"tceb3b"	"tkt"	"tln2"	"tmed8"	"tmf1"	"tobramycin"	"tpcn1"	"trpm4"	"trpv1"	"tsd"	"tshr"	"ttc21a"	"tumor"	"u2surp"	"ube3a"	"ubxn10"	"upf2"	"usp26"	"uty"	"vasp"	"vav2"	"vglut1"	"white-sutton syndrome"	"ws"	"znf142"	"znf280d"	"znf300"
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