Matches in Nanopublications for { ?s ?p "[This concise review is focused on genetic, molecular and clinical aspects of von Willebrand disease (VWD) type 2N and of mild hemophilia A due to mutations impairing FVIII-von Willebrand factor (VWF) interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_assertion description "[This concise review is focused on genetic, molecular and clinical aspects of von Willebrand disease (VWD) type 2N and of mild hemophilia A due to mutations impairing FVIII-von Willebrand factor (VWF) interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632626.RAa-S67eKBptvnDnmOP-agkUXCvT9YS41Y7W97rbx9jMA130_provenance.
- assertion description "[This concise review is focused on genetic, molecular and clinical aspects of von Willebrand disease (VWD) type 2N and of mild hemophilia A due to mutations impairing FVIII-von Willebrand factor (VWF) interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_assertion description "[This concise review is focused on genetic, molecular and clinical aspects of von Willebrand disease (VWD) type 2N and of mild hemophilia A due to mutations impairing FVIII-von Willebrand factor (VWF) interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_provenance.
- NP392293.RAkLS2k-dsZ8EUY7XPzhj8luZ3dKdXKFY_TM3DzUeZNBg130_assertion description "[This concise review is focused on genetic, molecular and clinical aspects of von Willebrand disease (VWD) type 2N and of mild hemophilia A due to mutations impairing FVIII-von Willebrand factor (VWF) interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392293.RAkLS2k-dsZ8EUY7XPzhj8luZ3dKdXKFY_TM3DzUeZNBg130_provenance.
- NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_assertion description "[This concise review is focused on genetic, molecular and clinical aspects of von Willebrand disease (VWD) type 2N and of mild hemophilia A due to mutations impairing FVIII-von Willebrand factor (VWF) interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_provenance.
- NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_assertion description "[This concise review is focused on genetic, molecular and clinical aspects of von Willebrand disease (VWD) type 2N and of mild hemophilia A due to mutations impairing FVIII-von Willebrand factor (VWF) interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_provenance.
- NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_assertion description "[This concise review is focused on genetic, molecular and clinical aspects of von Willebrand disease (VWD) type 2N and of mild hemophilia A due to mutations impairing FVIII-von Willebrand factor (VWF) interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_provenance.