Matches in Nanopublications for { ?s ?p "[A new variant of human prothrombin: prothrombin Metz, demonstration in a family showing double heterozygosity for congenital hypoprothrombinemia and dysprothrombinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP252532.RAKJO7n-luIMVsZeOpIBAnLbrv6OsIJ0IvDSGc4485uJQ130_assertion description "[A new variant of human prothrombin: prothrombin Metz, demonstration in a family showing double heterozygosity for congenital hypoprothrombinemia and dysprothrombinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252532.RAKJO7n-luIMVsZeOpIBAnLbrv6OsIJ0IvDSGc4485uJQ130_provenance.
- NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_assertion description "[A new variant of human prothrombin: prothrombin Metz, demonstration in a family showing double heterozygosity for congenital hypoprothrombinemia and dysprothrombinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_provenance.
- NP389681.RAKAuvQz9eapkKm-BcfZGB-7n1KDIsXzdADeC3H1Ul8-M130_assertion description "[A new variant of human prothrombin: prothrombin Metz, demonstration in a family showing double heterozygosity for congenital hypoprothrombinemia and dysprothrombinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389681.RAKAuvQz9eapkKm-BcfZGB-7n1KDIsXzdADeC3H1Ul8-M130_provenance.