About: covid:PMC7385101

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About: covid:PMC7385101 Goto Sponge NotDistinct Permalink

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

Attributes	Values
Creator	Wang, Xing Zheng, Lei Ma, Panpan Chen, Xue Ma, Xu Liu, Furong Cao, Zongfu Chen, Cuixia Feng, Xuan Hao, Shengju Zhang, Qinghua Zhang, Chuan Zhou, Bingbo
is schema:about of	named entity 'amino acid' named entity 'prenatal diagnosis' named entity 'cblB' named entity 'informed consent' named entity 'OMIM' named entity 'vitamin B12' named entity 'μmol/L' named entity 'valine' named entity 'OMIM' named entity 'MMADHC' named entity 'probands' named entity 'MMACHC' named entity 'amniotic fluid' named entity 'multisystem disease' named entity 'China' named entity 'Mutation screening' named entity 'MMAB' named entity 'China' named entity 'proband' named entity 'HCY' named entity 'OMIM' named entity 'Shandong Province' named entity 'pathogenesis' named entity 'OMIM' named entity 'blood samples' named entity 'behavioral disorders' named entity 'functional analysis' named entity 'clinical symptoms' named entity 'methylmalonyl-CoA epimerase' named entity 'compound heterozygous' named entity 'MS/MS' named entity 'family 7' named entity 'compound heterozygous' named entity 'MMACHC' named entity 'family 7' named entity 'serum' named entity 'cblF' named entity 'organic acids' named entity 'OMIM' named entity 'Sanger sequencing' named entity 'biochemical' named entity 'Family 7' named entity 'pregnancy' named entity 'follow-up' named entity 'Newborn screening' named entity 'folate' named entity 'inborn errors of metabolism' named entity 'family 7' named entity 'alleles' named entity 'MS/MS' named entity 'GC/MS' named entity 'next-generation sequencing' named entity 'cbl' named entity 'μmol/L' named entity 'MMACHC' named entity 'MMACHC' named entity 'homozygous' named entity 'ClinVar' named entity 'MMAB' named entity 'Health Care' named entity 'LMBRD1' named entity 'metabolic acidosis' named entity 'MMACHC' named entity 'prenatal diagnosis' named entity 'MMACHC' named entity 'compound heterozygous' named entity 'consanguineous families' named entity 'prognosis' named entity 'pregnancy' named entity 'mutation' named entity 'genetic counseling' named entity 'Wechsler Intelligence Scale for Children' named entity 'folate' named entity 'phenotype' named entity 'cobalamin' named entity 'cobalamin' named entity 'homozygous' named entity 'China' named entity 'pathogenicity' named entity 'molecular diagnosis' named entity 'fetus' named entity 'China' named entity 'metabolic acidosis' named entity 'Beijing' named entity 'threonine' named entity 'prenatal diagnosis' named entity 'neonatal period'

Attributes

Values

Creator

Wang, Xing
Zheng, Lei
Ma, Panpan
Chen, Xue
Ma, Xu
Liu, Furong
Cao, Zongfu
Chen, Cuixia
Feng, Xuan
Hao, Shengju
Zhang, Qinghua
Zhang, Chuan
Zhou, Bingbo

is schema:about of

named entity 'amino acid'
named entity 'prenatal diagnosis'
named entity 'cblB'
named entity 'informed consent'
named entity 'OMIM'
named entity 'vitamin B12'
named entity 'μmol/L'
named entity 'valine'
named entity 'OMIM'
named entity 'MMADHC'
named entity 'probands'
named entity 'MMACHC'
named entity 'amniotic fluid'
named entity 'multisystem disease'
named entity 'China'
named entity 'Mutation screening'
named entity 'MMAB'
named entity 'China'
named entity 'proband'
named entity 'HCY'
named entity 'OMIM'
named entity 'Shandong Province'
named entity 'pathogenesis'
named entity 'OMIM'
named entity 'blood samples'
named entity 'behavioral disorders'
named entity 'functional analysis'
named entity 'clinical symptoms'
named entity 'methylmalonyl-CoA epimerase'
named entity 'compound heterozygous'
named entity 'MS/MS'
named entity 'family 7'
named entity 'compound heterozygous'
named entity 'MMACHC'
named entity 'family 7'
named entity 'serum'
named entity 'cblF'
named entity 'organic acids'
named entity 'OMIM'
named entity 'Sanger sequencing'
named entity 'biochemical'
named entity 'Family 7'
named entity 'pregnancy'
named entity 'follow-up'
named entity 'Newborn screening'
named entity 'folate'
named entity 'inborn errors of metabolism'
named entity 'family 7'
named entity 'alleles'
named entity 'MS/MS'
named entity 'GC/MS'
named entity 'next-generation sequencing'
named entity 'cbl'
named entity 'μmol/L'
named entity 'MMACHC'
named entity 'MMACHC'
named entity 'homozygous'
named entity 'ClinVar'
named entity 'MMAB'
named entity 'Health Care'
named entity 'LMBRD1'
named entity 'metabolic acidosis'
named entity 'MMACHC'
named entity 'prenatal diagnosis'
named entity 'MMACHC'
named entity 'compound heterozygous'
named entity 'consanguineous families'
named entity 'prognosis'
named entity 'pregnancy'
named entity 'mutation'
named entity 'genetic counseling'
named entity 'Wechsler Intelligence Scale for Children'
named entity 'folate'
named entity 'phenotype'
named entity 'cobalamin'
named entity 'cobalamin'
named entity 'homozygous'
named entity 'China'
named entity 'pathogenicity'
named entity 'molecular diagnosis'
named entity 'fetus'
named entity 'China'
named entity 'metabolic acidosis'
named entity 'Beijing'
named entity 'threonine'
named entity 'prenatal diagnosis'
named entity 'neonatal period'

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