Nanopublications

Matches in Nanopublications for { ?s ?p "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

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NP178229.RA1MWJAo6u1aToEGQgGAub_-rZvN-Got6fPxNU227HDyM130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178229.RA1MWJAo6u1aToEGQgGAub_-rZvN-Got6fPxNU227HDyM130_provenance.
NP223619.RA4YLZTaQSNLbsI1k64kzam1mgU9OOCTqexP0l-hdDLFg130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223619.RA4YLZTaQSNLbsI1k64kzam1mgU9OOCTqexP0l-hdDLFg130_provenance.
NP247351.RA7B5-gz6rRu4Qgb1AQO9kKQz4YMp9n4ZQEstFq0vXhkg130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247351.RA7B5-gz6rRu4Qgb1AQO9kKQz4YMp9n4ZQEstFq0vXhkg130_provenance.
NP343097.RAgc9PFtpW03Enz05wPw-jnBDwEascusWpoQFoaHEKqL0130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343097.RAgc9PFtpW03Enz05wPw-jnBDwEascusWpoQFoaHEKqL0130_provenance.
NP220430.RAszIVW5NCZEi8NMRVxGUOCXEaQbj374XBp7IquuIHrBg130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220430.RAszIVW5NCZEi8NMRVxGUOCXEaQbj374XBp7IquuIHrBg130_provenance.
NP457402.RAXafCqnEiCk4xOCUsJ5Bpa4kZkAwto0knkI3WWuLNizA130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP457402.RAXafCqnEiCk4xOCUsJ5Bpa4kZkAwto0knkI3WWuLNizA130_provenance.
NP756897.RARjH7zugTgdG7D8GYvL8gHtdQC-R44axL-Sf5cVPD-cM130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756897.RARjH7zugTgdG7D8GYvL8gHtdQC-R44axL-Sf5cVPD-cM130_provenance.
assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
NP496651.RA6U2zp-yMyLwlxjOkzpz7BHNMYEfFI1gM-oW0jyPkb1o130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496651.RA6U2zp-yMyLwlxjOkzpz7BHNMYEfFI1gM-oW0jyPkb1o130_provenance.
assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
NP382399.RAWd5JxuocYvS4haC0e_ot-Ogqu5NL5YYatj1MZ43TMxQ130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382399.RAWd5JxuocYvS4haC0e_ot-Ogqu5NL5YYatj1MZ43TMxQ130_provenance.
NP441719.RAQxqolB6aQZ6VhB7N18CLxbD0gp1Z7nkpobNXjIPA1Zo130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441719.RAQxqolB6aQZ6VhB7N18CLxbD0gp1Z7nkpobNXjIPA1Zo130_provenance.
NP547002.RAFqndb35OLNuzDW0zVtxdxuSCOLDXgPTqvq8Zp5x2xJY130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547002.RAFqndb35OLNuzDW0zVtxdxuSCOLDXgPTqvq8Zp5x2xJY130_provenance.
NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_provenance.
NP638953.RAIA0SMnm4ML75sYiZk_W9ubIPfkMmy4l3K_o8VIYRA6w130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP638953.RAIA0SMnm4ML75sYiZk_W9ubIPfkMmy4l3K_o8VIYRA6w130_provenance.
NP1009754.RAYQRaGqtR-rdxamLyjXDw2wNF9rum579swKmGSxHKhXk130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009754.RAYQRaGqtR-rdxamLyjXDw2wNF9rum579swKmGSxHKhXk130_provenance.
NP1009766.RAWwjQRHDWLBcWUTb8VQ9yQTsDckrjyqoFXS-ndPG5DHA130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009766.RAWwjQRHDWLBcWUTb8VQ9yQTsDckrjyqoFXS-ndPG5DHA130_provenance.
NP1011261.RAA2RUzh9R3ZQTO-4slU5fpB3FlDLm0vH5a_SWVSoj3Vo130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011261.RAA2RUzh9R3ZQTO-4slU5fpB3FlDLm0vH5a_SWVSoj3Vo130_provenance.
NP351885.RAdt4N86HZ0gp_iXKgLggs7O2uoKfGCkOzxppjlV21oQ0130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351885.RAdt4N86HZ0gp_iXKgLggs7O2uoKfGCkOzxppjlV21oQ0130_provenance.
NP351887.RAfVTfcWBo8W1EnlRjZ554GN389VQ2nZZoKtIxk23aizo130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351887.RAfVTfcWBo8W1EnlRjZ554GN389VQ2nZZoKtIxk23aizo130_provenance.
NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_provenance.
NP351890.RAY8I7T1dib9RhamwyeH-yMCBvg2lJGN6c6RxUw9OKoHQ130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351890.RAY8I7T1dib9RhamwyeH-yMCBvg2lJGN6c6RxUw9OKoHQ130_provenance.
assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
NP441555.RAl44vN0EPKSMsyORJILdDEKrCQqnxFQensrIQAU8gpeo130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441555.RAl44vN0EPKSMsyORJILdDEKrCQqnxFQensrIQAU8gpeo130_provenance.
NP441711.RAsh_hZyq8ccakcx49S3OCZwEPHxS0qLRBJgfpMYnbcf0130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441711.RAsh_hZyq8ccakcx49S3OCZwEPHxS0qLRBJgfpMYnbcf0130_provenance.
NP351888.RAptj-9PUZYoTZeIg0v98L5XRtCnu2vi5tpKWkkjnzGhU130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351888.RAptj-9PUZYoTZeIg0v98L5XRtCnu2vi5tpKWkkjnzGhU130_provenance.
NP381852.RA6lPo_64dSt02Mbw47qCuROesyQNyFeTNMIwkvg25jYM130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381852.RA6lPo_64dSt02Mbw47qCuROesyQNyFeTNMIwkvg25jYM130_provenance.
NP441648.RA6HgAqiD5Y_HusYcoJSFn7ry8RjJ5JNki-syzLS10PZc130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441648.RA6HgAqiD5Y_HusYcoJSFn7ry8RjJ5JNki-syzLS10PZc130_provenance.
NP441660.RAyzcDsvTFsF2UVqXjuqqANzGQSkgHZInHUzmbLtbbm-c130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441660.RAyzcDsvTFsF2UVqXjuqqANzGQSkgHZInHUzmbLtbbm-c130_provenance.
NP441768.RAyxt-YqkA-YxEdyWE76veYXmgDf5wl6s1a5NUQVYnU1E130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441768.RAyxt-YqkA-YxEdyWE76veYXmgDf5wl6s1a5NUQVYnU1E130_provenance.
NP441542.RAIX9vx_6FKkeClk_3zJJZR_D5XjRV4RfrhxwePkJsx0g130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441542.RAIX9vx_6FKkeClk_3zJJZR_D5XjRV4RfrhxwePkJsx0g130_provenance.
NP441758.RAF9DtN5BloTCVytJw4Y2XQhe_9qJ5ESwmuyM_qmkZ8lE130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441758.RAF9DtN5BloTCVytJw4Y2XQhe_9qJ5ESwmuyM_qmkZ8lE130_provenance.
NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_provenance.
NP992089.RAz9TkrSlFNg4f_VAKD8tV1lE0CRaAT8pwxe4ZnVXO694130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP992089.RAz9TkrSlFNg4f_VAKD8tV1lE0CRaAT8pwxe4ZnVXO694130_provenance.
NP351883.RA43bFU6WOKrefLxUScOBTW96XlGrZ-PWpV5I5Qo_SqlA130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351883.RA43bFU6WOKrefLxUScOBTW96XlGrZ-PWpV5I5Qo_SqlA130_provenance.
NP351884.RA0GvaiaKAEoaxGi2e3TmEk3_e_1Dq2HbOxKo3Lt5IXsg130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351884.RA0GvaiaKAEoaxGi2e3TmEk3_e_1Dq2HbOxKo3Lt5IXsg130_provenance.
NP351886.RAxb7zJZmRekLAIxVOm9Z1nPBNacrHWsNe42u4CQxyYno130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351886.RAxb7zJZmRekLAIxVOm9Z1nPBNacrHWsNe42u4CQxyYno130_provenance.
NP351891.RAyDgvuXtcZcFNaVA1oMFfwEYx6uZ99hPb_kFCmXo-FI0130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351891.RAyDgvuXtcZcFNaVA1oMFfwEYx6uZ99hPb_kFCmXo-FI0130_provenance.