Matches in Nanopublications for { ?s ?p "[a rare polymorphism at codon 171 (Asn-- > Ser) of human Prnp is associated with symptomatic epilepsies related to different forms of malformations of cortical development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_assertion description "[a rare polymorphism at codon 171 (Asn-- > Ser) of human Prnp is associated with symptomatic epilepsies related to different forms of malformations of cortical development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_provenance.
- NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_assertion description "[a rare polymorphism at codon 171 (Asn-- > Ser) of human Prnp is associated with symptomatic epilepsies related to different forms of malformations of cortical development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_provenance.
- NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_assertion description "[a rare polymorphism at codon 171 (Asn-- > Ser) of human Prnp is associated with symptomatic epilepsies related to different forms of malformations of cortical development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_provenance.
- assertion description "[a rare polymorphism at codon 171 (Asn-- > Ser) of human Prnp is associated with symptomatic epilepsies related to different forms of malformations of cortical development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.