Matches in Nanopublications for { ?s ?p "[Mutations in LMAN1 (also called ERGIC-53) result in combined deficiency of factor V and factor VIII (F5F8D), an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP287668.RAjxsIDV3351D55DoS7LbaXwqoh6TajYHbYD5wQtzOLtE130_assertion description "[Mutations in LMAN1 (also called ERGIC-53) result in combined deficiency of factor V and factor VIII (F5F8D), an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP287668.RAjxsIDV3351D55DoS7LbaXwqoh6TajYHbYD5wQtzOLtE130_provenance.
- NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_assertion description "[Mutations in LMAN1 (also called ERGIC-53) result in combined deficiency of factor V and factor VIII (F5F8D), an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583842.RAfrpTZFgWoCDR2n4IDu4zWi4wUqnhaUVcKQsPlObs_Og130_provenance.
- assertion description "[Mutations in LMAN1 (also called ERGIC-53) result in combined deficiency of factor V and factor VIII (F5F8D), an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in LMAN1 (also called ERGIC-53) result in combined deficiency of factor V and factor VIII (F5F8D), an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP392519.RAeWsgLXFSHsQBcQ0qPqa4EZec-TxK4q0h4fSC8f3_pvo130_assertion description "[Mutations in LMAN1 (also called ERGIC-53) result in combined deficiency of factor V and factor VIII (F5F8D), an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392519.RAeWsgLXFSHsQBcQ0qPqa4EZec-TxK4q0h4fSC8f3_pvo130_provenance.
- NP392520.RAVDTR7r6e0AoYNte9QrFZ4MYqEofoJzRoyGAsXg792iY130_assertion description "[Mutations in LMAN1 (also called ERGIC-53) result in combined deficiency of factor V and factor VIII (F5F8D), an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392520.RAVDTR7r6e0AoYNte9QrFZ4MYqEofoJzRoyGAsXg792iY130_provenance.
- assertion description "[Mutations in LMAN1 (also called ERGIC-53) result in combined deficiency of factor V and factor VIII (F5F8D), an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP960241.RAkVdED5bV-kqJ-0c3gypaQg4pYoLPGRkFf_C1Xwzgu0c130_assertion description "[Mutations in LMAN1 (also called ERGIC-53) result in combined deficiency of factor V and factor VIII (F5F8D), an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960241.RAkVdED5bV-kqJ-0c3gypaQg4pYoLPGRkFf_C1Xwzgu0c130_provenance.
- NP537205.RA2hl8RdAvLTFhVx-pXR07Rj1ECnuiTaXiuKxCYYV5fdM130_assertion description "[Mutations in LMAN1 (also called ERGIC-53) result in combined deficiency of factor V and factor VIII (F5F8D), an autosomal recessive bleeding disorder characterized by coordinate reduction of both clotting proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537205.RA2hl8RdAvLTFhVx-pXR07Rj1ECnuiTaXiuKxCYYV5fdM130_provenance.