Matches in Nanopublications for { ?s ?p "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_assertion description "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance.
- NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_assertion description "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_provenance.
- NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_assertion description "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776378.RAZgUnpdgrXZiCb_g9Dmf2xEtDh_wtKO8AJQ3QeD_UpJ0130_provenance.
- assertion description "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_assertion description "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323280.RANQnd_--DjnqiMcvNfb4NRJC4lLdoTrFi7h5fOMUepvY130_provenance.
- NP1400781.RAS9vVZZFcnVkSfU_sZ1xxMjJVEC-2CWJ2lybZYFWBJkg130_assertion description "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1400781.RAS9vVZZFcnVkSfU_sZ1xxMjJVEC-2CWJ2lybZYFWBJkg130_provenance.
- NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_assertion description "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_provenance.
- assertion description "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.