Matches in Nanopublications for { ?s ?p "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP160030.RAH-IrHZYvg4cRvb8tUEhgXewF2vTP5MLK_ln9DoZM30A130_assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP160030.RAH-IrHZYvg4cRvb8tUEhgXewF2vTP5MLK_ln9DoZM30A130_provenance.
- assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382416.RAS6JkBffEM4ZY1CQTGY6vnaaaxH2xE3fl7M6FacEILQ8130_provenance.
- NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_provenance.
- NP1072813.RAs81EdTH0pnQ4OuOAwPW7BTUzfZHoyjcWEb6YFgIxDUc130_assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1072813.RAs81EdTH0pnQ4OuOAwPW7BTUzfZHoyjcWEb6YFgIxDUc130_provenance.
- NP1072814.RAo1XW6tproTiUn8ze_B94d7aIXfIg7mMpZKizVpcfZgk130_assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1072814.RAo1XW6tproTiUn8ze_B94d7aIXfIg7mMpZKizVpcfZgk130_provenance.
- NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_provenance.
- NP1072816.RA0MDf7Rxo8gV4iy8yrYSJ5uGJr6El7BlG9IaZuevib-w130_assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1072816.RA0MDf7Rxo8gV4iy8yrYSJ5uGJr6El7BlG9IaZuevib-w130_provenance.