Matches in Nanopublications for { ?s ?p "[A deletion-insertion mutation in the phosphomannomutase 2 gene in an African American patient with congenital disorders of glycosylation-Ia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP246964.RA1OhK5VNSSLX_WHOGZVlzYuAYUJz7P9oPkI58qENfwI4130_assertion description "[A deletion-insertion mutation in the phosphomannomutase 2 gene in an African American patient with congenital disorders of glycosylation-Ia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246964.RA1OhK5VNSSLX_WHOGZVlzYuAYUJz7P9oPkI58qENfwI4130_provenance.
- NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_assertion description "[A deletion-insertion mutation in the phosphomannomutase 2 gene in an African American patient with congenital disorders of glycosylation-Ia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632247.RADMAfT064tOyM03bdeioTL3YjsnPpvAL252Pseyhmom4130_provenance.
- NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_assertion description "[A deletion-insertion mutation in the phosphomannomutase 2 gene in an African American patient with congenital disorders of glycosylation-Ia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347930.RAUvJER9pSklpzmZr8DUjk-E4p38jGOMrKqSWvn6_u-LU130_provenance.