Matches in Nanopublications for { ?s ?p "[A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_assertion description "[A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_provenance.
- NP6550.RADr7Qg3UKhiyEyIfqXV4arlv88QHe7f3rpOQTWY7H_mQ130_assertion description "[A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6550.RADr7Qg3UKhiyEyIfqXV4arlv88QHe7f3rpOQTWY7H_mQ130_provenance.
- NP1331181.RACYK1vQ6CryXSQPG8s18RTCOEdn4TyfS1V9u0TIDtGKI130_assertion description "[A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1331181.RACYK1vQ6CryXSQPG8s18RTCOEdn4TyfS1V9u0TIDtGKI130_provenance.
- NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_assertion description "[A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_provenance.