Matches in Nanopublications for { ?s ?p "[Most children have severe developmental delay and infantile spasms, but milder phenotypes are on record, including posterior SBH owing to mosaic mutations of LIS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- assertion description "[Most children have severe developmental delay and infantile spasms, but milder phenotypes are on record, including posterior SBH owing to mosaic mutations of LIS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP551505.RASAaoby3yyiggZv-tgNlmmHmZ1DbmNlvTE2ch0C-KCHA130_assertion description "[Most children have severe developmental delay and infantile spasms, but milder phenotypes are on record, including posterior SBH owing to mosaic mutations of LIS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551505.RASAaoby3yyiggZv-tgNlmmHmZ1DbmNlvTE2ch0C-KCHA130_provenance.
- NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_assertion description "[Most children have severe developmental delay and infantile spasms, but milder phenotypes are on record, including posterior SBH owing to mosaic mutations of LIS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606199.RAuWrSV2otfRWdXDAzZe2QgNAuHiydpPuOmb7cDykqBMk130_provenance.
- NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_assertion description "[Most children have severe developmental delay and infantile spasms, but milder phenotypes are on record, including posterior SBH owing to mosaic mutations of LIS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606032.RA0_cQkdYe-gRo1a8jrYcYtdMqfmHdJ7OBxOLbHbWw10s130_provenance.
- NP551502.RAM0reZmY8tqK4t8yt8BxzovUgeXIzabox48cSubulx0E130_assertion description "[Most children have severe developmental delay and infantile spasms, but milder phenotypes are on record, including posterior SBH owing to mosaic mutations of LIS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551502.RAM0reZmY8tqK4t8yt8BxzovUgeXIzabox48cSubulx0E130_provenance.