Matches in Nanopublications for { ?s ?p "[We expand the mutational spectrum in patients with FOXG1-related encephalopathies and precise the core FOXG1 syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[We expand the mutational spectrum in patients with FOXG1-related encephalopathies and precise the core FOXG1 syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_assertion description "[We expand the mutational spectrum in patients with FOXG1-related encephalopathies and precise the core FOXG1 syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_provenance.
- NP404363.RAjIj0fqw-pbIJHwD20zbE1B39i77jjoH2Eryqzx1RN_s130_assertion description "[We expand the mutational spectrum in patients with FOXG1-related encephalopathies and precise the core FOXG1 syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404363.RAjIj0fqw-pbIJHwD20zbE1B39i77jjoH2Eryqzx1RN_s130_provenance.