Matches in Nanopublications for { ?s ?p "[Phenylketonuria (PKU) is characterized by persistent hyperphenylalaninemia, due to mutations in the gene coding for phenylalanine hydroxylase (PAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_assertion description "[Phenylketonuria (PKU) is characterized by persistent hyperphenylalaninemia, due to mutations in the gene coding for phenylalanine hydroxylase (PAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557365.RA_h3-G722mkTvTSyVFK5weIDHbTsD3e6Py2sltKzY_3Q130_provenance.
- NP838330.RAB90pn-BaLbSOFoXLBaifQKTiTu5K0oE2Rf1uOusAt6g130_assertion description "[Phenylketonuria (PKU) is characterized by persistent hyperphenylalaninemia, due to mutations in the gene coding for phenylalanine hydroxylase (PAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838330.RAB90pn-BaLbSOFoXLBaifQKTiTu5K0oE2Rf1uOusAt6g130_provenance.
- NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_assertion description "[Phenylketonuria (PKU) is characterized by persistent hyperphenylalaninemia, due to mutations in the gene coding for phenylalanine hydroxylase (PAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838329.RA-YO6t0Et_TMWH5bzdBPo6HahNVokiJauCM0m9qxGfhk130_provenance.
- assertion description "[Phenylketonuria (PKU) is characterized by persistent hyperphenylalaninemia, due to mutations in the gene coding for phenylalanine hydroxylase (PAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_assertion description "[Phenylketonuria (PKU) is characterized by persistent hyperphenylalaninemia, due to mutations in the gene coding for phenylalanine hydroxylase (PAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_provenance.
- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion description "[Phenylketonuria (PKU) is characterized by persistent hyperphenylalaninemia, due to mutations in the gene coding for phenylalanine hydroxylase (PAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.