About: covid:08e8cd9cddb6f5f55f2f08a36fb5458c3d643344

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About: covid:08e8cd9cddb6f5f55f2f08a36fb5458c3d643344 Goto Sponge NotDistinct Permalink

An Entity of Type : owl:Thing, within Data Space : wasabi.inria.fr associated with source document(s)

Attributes	Values
Creator	Alexander, • Barešić, Anja Dahoun, Tarik Howes, • Lenhard, Boris Nash, Jolyon
is schema:about of	named entity 'genes' named entity 'linking' named entity 'study' named entity 'tool' named entity 'genetics' named entity 'PREDICTED' named entity 'POTENTIAL' named entity 'MAJORITY' named entity 'STRENGTH' named entity 'ANALYSIS' named entity 'CONTEXT' named entity 'IDENTIFIED' named entity 'HERE' named entity 'LINKING' named entity 'AUTISM SPECTRUM DISORDER' named entity 'genomic' named entity 'non-coding regions' named entity 'detect' named entity 'SNP' named entity 'fact' named entity 'arrays' named entity 'genes' named entity 'gene' named entity 'regions' named entity 'genome-wide association studies' named entity 'conserved' named entity 'Our' named entity 'bipolar' named entity 'developmental disorders' named entity 'Understanding' named entity 'enhancer' named entity 'GWAS' named entity 'schizophrenia' named entity 'GWAS' named entity 'bipolar disorder' named entity 'genomic regulatory' named entity 'neuropsychiatric disorders' named entity 'disorder' named entity 'enhancer' named entity 'IRX3' named entity 'genomic regulatory' named entity 'schizophrenia' named entity 'enhancers' named entity 'gene' named entity 'GWAS' named entity 'DRD2' named entity 'gene' named entity 'genome' named entity 'control group' named entity 'bipolar disorder' named entity 'chromatin' named entity 'SNP' named entity 'SNPs' named entity 'phenotypes' named entity 'loci' named entity 'regulatory elements' named entity 'brain abnormalities' named entity 'ZEB2' named entity 'GWAS' named entity 'linkage disequilibrium' named entity 'gene families' named entity 'molecular mechanisms' named entity 'entropy' named entity 'genomic regulatory' named entity 'loci' named entity 'cell adhesion molecules' named entity 'intellectual disability' named entity 'loci' named entity 'gene' named entity 'genome' named entity 'non-coding regions' named entity 'TADs' named entity 'transcription' named entity 'disease mechanisms' named entity 'BCL11A' named entity 'GWAS' named entity 'enhancers' named entity 'GWAS' named entity 'genome' named entity 'genome-wide association studies' named entity 'Hi-C' named entity 'missing heritability' named entity 'aetiology' named entity 'enhancers' named entity 'SNP' named entity 'non-coding' named entity 'genome' named entity 'dorsolateral prefrontal cortex' named entity 'ZEB2' named entity 'base pairs' named entity 'SNPs' named entity 'gene' named entity 'loci' named entity 'Springer Nature'

Attributes

Values

Creator

Alexander, •
Barešić, Anja
Dahoun, Tarik
Howes, •
Lenhard, Boris
Nash, Jolyon

is schema:about of

named entity 'genes'
named entity 'linking'
named entity 'study'
named entity 'tool'
named entity 'genetics'
named entity 'PREDICTED'
named entity 'POTENTIAL'
named entity 'MAJORITY'
named entity 'STRENGTH'
named entity 'ANALYSIS'
named entity 'CONTEXT'
named entity 'IDENTIFIED'
named entity 'HERE'
named entity 'LINKING'
named entity 'AUTISM SPECTRUM DISORDER'
named entity 'genomic'
named entity 'non-coding regions'
named entity 'detect'
named entity 'SNP'
named entity 'fact'
named entity 'arrays'
named entity 'genes'
named entity 'gene'
named entity 'regions'
named entity 'genome-wide association studies'
named entity 'conserved'
named entity 'Our'
named entity 'bipolar'
named entity 'developmental disorders'
named entity 'Understanding'
named entity 'enhancer'
named entity 'GWAS'
named entity 'schizophrenia'
named entity 'GWAS'
named entity 'bipolar disorder'
named entity 'genomic regulatory'
named entity 'neuropsychiatric disorders'
named entity 'disorder'
named entity 'enhancer'
named entity 'IRX3'
named entity 'genomic regulatory'
named entity 'schizophrenia'
named entity 'enhancers'
named entity 'gene'
named entity 'GWAS'
named entity 'DRD2'
named entity 'gene'
named entity 'genome'
named entity 'control group'
named entity 'bipolar disorder'
named entity 'chromatin'
named entity 'SNP'
named entity 'SNPs'
named entity 'phenotypes'
named entity 'loci'
named entity 'regulatory elements'
named entity 'brain abnormalities'
named entity 'ZEB2'
named entity 'GWAS'
named entity 'linkage disequilibrium'
named entity 'gene families'
named entity 'molecular mechanisms'
named entity 'entropy'
named entity 'genomic regulatory'
named entity 'loci'
named entity 'cell adhesion molecules'
named entity 'intellectual disability'
named entity 'loci'
named entity 'gene'
named entity 'genome'
named entity 'non-coding regions'
named entity 'TADs'
named entity 'transcription'
named entity 'disease mechanisms'
named entity 'BCL11A'
named entity 'GWAS'
named entity 'enhancers'
named entity 'GWAS'
named entity 'genome'
named entity 'genome-wide association studies'
named entity 'Hi-C'
named entity 'missing heritability'
named entity 'aetiology'
named entity 'enhancers'
named entity 'SNP'
named entity 'non-coding'
named entity 'genome'
named entity 'dorsolateral prefrontal cortex'
named entity 'ZEB2'
named entity 'base pairs'
named entity 'SNPs'
named entity 'gene'
named entity 'loci'
named entity 'Springer Nature'

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