Matches in Nanopublications for { ?s ?p "[Screening for Fabry disease (FD), an X-linked lysosomal storage disorder, reveals a significant number of individuals with a genetic variant of unknown significance without classical FD manifestations; these variants in the ?-galactosidase A gene often result in a high residual leukocyte ?-galactosidase A and it is unclear whether these individuals suffer from FD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Screening for Fabry disease (FD), an X-linked lysosomal storage disorder, reveals a significant number of individuals with a genetic variant of unknown significance without classical FD manifestations; these variants in the ?-galactosidase A gene often result in a high residual leukocyte ?-galactosidase A and it is unclear whether these individuals suffer from FD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1216677.RAcQSp6bHCCYuddddaqB5T9wzLEJM6D8GRUvhbnFcPwxU130_assertion description "[Screening for Fabry disease (FD), an X-linked lysosomal storage disorder, reveals a significant number of individuals with a genetic variant of unknown significance without classical FD manifestations; these variants in the ?-galactosidase A gene often result in a high residual leukocyte ?-galactosidase A and it is unclear whether these individuals suffer from FD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216677.RAcQSp6bHCCYuddddaqB5T9wzLEJM6D8GRUvhbnFcPwxU130_provenance.