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K Stals
K Stals
Item
http://www.wikidata.org/entity/Q87982778
Q87982778
about
Diagnosis of lethal or prenatal-onset autosomal recessive disorders by parental exome sequencing.
Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy.
P50
Q47863563-272C605A-0DE5-4545-87A4-9187CFE25BB2
Q50420610-C8275F29-08F5-4EB8-A6C2-250A12FA6EF9
P50
K Stals
Item
http://www.wikidata.org/entity/Q87982778
description
researcher
@en
wetenschapper
@nl
name
K Stals
@en
K Stals
@nl
type
Item
label
K Stals
@en
K Stals
@nl
prefLabel
K Stals
@en
K Stals
@nl
P31
Q87982778-5A5BFAEB-10AF-4892-BF11-1526D8F07762
P496
Q87982778-18C8DA89-14EF-40E5-98DD-DB0A9D41DC55
P496
0000-0002-3255-7044
P31
Afgan
P496
0000-0002-3255-7044
http://www.w3.org/2001/XMLSchema#string