About: covid:PMC7102302

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About: covid:PMC7102302 Goto Sponge NotDistinct Permalink

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

Attributes	Values
Creator	Junker, Anne Embree, Joanne Langley, Joanne Grenier, Danielle Haddad, Elie Long, Richard Ramsingh, Rose Rozmus, Jacob Schultz, Kirk Singh, Veeran-Anne Thibodeau, Melanie Turvey, Stuart Yacoub, Wadieh
is schema:about of	named entity 'Canadian' named entity 'Severe Combined Immunodeficiency' named entity 'gene therapy' named entity 'Canadian' named entity 'BCG vaccine' named entity 'chronic diarrhea' named entity 'neonatal screening' named entity 'BCG' named entity 'Canadian' named entity 'First Nations' named entity 'MHC Class II' named entity 'genetic mutations' named entity 'ALC' named entity 'early diagnosis' named entity 'ADA deficiency' named entity 'pediatric' named entity 'SCID' named entity 'First Nations' named entity 'MHC class II' named entity 'risk factors' named entity 'BCG' named entity 'HSCT' named entity 'Canadian' named entity 'SCID' named entity 'family history' named entity 'SCID' named entity 'Universal screening' named entity 'ALC' named entity 'family history' named entity 'interferon gamma' named entity 'ALC' named entity 'X-linked SCID' named entity 'respiratory failure' named entity 'First Nations' named entity 'failure to thrive' named entity 'gene therapy' named entity 'RAG1' named entity 'end-organ' named entity 'Canadian' named entity 'ESID' named entity 'SCID' named entity 'newborn screening' named entity 'Tuberculosis' named entity 'SCID' named entity 'SCID' named entity 'family history' named entity 'T-cell' named entity 'BCG' named entity 'diagnostic criteria' named entity 'clinical findings' named entity 'Canadian Pediatric Society' named entity 'hematopoietic stem cell transplantation' named entity 'failure to thrive' named entity 'SCID' named entity 'BCG' named entity 'newborn screening' named entity 'primary immunodeficiencies' named entity 'SCID' named entity 'missing data' named entity 'incidence rate' named entity 'Immunodeficiency' named entity 'family history' named entity 'neonatal' named entity 'MHC class II' named entity 'immune function' named entity 'SCID' named entity 'allogeneic hematopoietic stem cell transplantation' named entity 'Inuit' named entity 'infant deaths' named entity 'ALC' named entity 'consanguinity' named entity 'consanguinity' named entity 'SCID' named entity 'skewed distribution' named entity 'cohort study' named entity 'Aboriginal identity' named entity 'France' named entity 'Athabascan' named entity 'SCID' named entity 'placental' named entity 'risk factors' named entity 'Canada' named entity 'clinical features' named entity 'public health' named entity '3.5' named entity 'genetic mutation' named entity 'Hematopoietic stem cell transplantation'

Attributes

Values

Creator

Junker, Anne
Embree, Joanne
Langley, Joanne
Grenier, Danielle
Haddad, Elie
Long, Richard
Ramsingh, Rose
Rozmus, Jacob
Schultz, Kirk
Singh, Veeran-Anne
Thibodeau, Melanie
Turvey, Stuart
Yacoub, Wadieh

is schema:about of

named entity 'Canadian'
named entity 'Severe Combined Immunodeficiency'
named entity 'gene therapy'
named entity 'Canadian'
named entity 'BCG vaccine'
named entity 'chronic diarrhea'
named entity 'neonatal screening'
named entity 'BCG'
named entity 'Canadian'
named entity 'First Nations'
named entity 'MHC Class II'
named entity 'genetic mutations'
named entity 'ALC'
named entity 'early diagnosis'
named entity 'ADA deficiency'
named entity 'pediatric'
named entity 'SCID'
named entity 'First Nations'
named entity 'MHC class II'
named entity 'risk factors'
named entity 'BCG'
named entity 'HSCT'
named entity 'Canadian'
named entity 'SCID'
named entity 'family history'
named entity 'SCID'
named entity 'Universal screening'
named entity 'ALC'
named entity 'family history'
named entity 'interferon gamma'
named entity 'ALC'
named entity 'X-linked SCID'
named entity 'respiratory failure'
named entity 'First Nations'
named entity 'failure to thrive'
named entity 'gene therapy'
named entity 'RAG1'
named entity 'end-organ'
named entity 'Canadian'
named entity 'ESID'
named entity 'SCID'
named entity 'newborn screening'
named entity 'Tuberculosis'
named entity 'SCID'
named entity 'SCID'
named entity 'family history'
named entity 'T-cell'
named entity 'BCG'
named entity 'diagnostic criteria'
named entity 'clinical findings'
named entity 'Canadian Pediatric Society'
named entity 'hematopoietic stem cell transplantation'
named entity 'failure to thrive'
named entity 'SCID'
named entity 'BCG'
named entity 'newborn screening'
named entity 'primary immunodeficiencies'
named entity 'SCID'
named entity 'missing data'
named entity 'incidence rate'
named entity 'Immunodeficiency'
named entity 'family history'
named entity 'neonatal'
named entity 'MHC class II'
named entity 'immune function'
named entity 'SCID'
named entity 'allogeneic hematopoietic stem cell transplantation'
named entity 'Inuit'
named entity 'infant deaths'
named entity 'ALC'
named entity 'consanguinity'
named entity 'consanguinity'
named entity 'SCID'
named entity 'skewed distribution'
named entity 'cohort study'
named entity 'Aboriginal identity'
named entity 'France'
named entity 'Athabascan'
named entity 'SCID'
named entity 'placental'
named entity 'risk factors'
named entity 'Canada'
named entity 'clinical features'
named entity 'public health'
named entity '3.5'
named entity 'genetic mutation'
named entity 'Hematopoietic stem cell transplantation'

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