Matches in Nanopublications for { ?s ?p "[Missense mutations in the FVIII gene impairing the binding to VWF are a common cause of mild/moderate hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP391346.RAW3OW4aYVNvuLtYI9WcbzEGBbxoRCFRbalTmCVr7GL7w130_assertion description "[Missense mutations in the FVIII gene impairing the binding to VWF are a common cause of mild/moderate hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391346.RAW3OW4aYVNvuLtYI9WcbzEGBbxoRCFRbalTmCVr7GL7w130_provenance.
- NP858348.RAW5bRaUVMLLaD7OrCIaJbEi3o5bijOqFZu6PRIFyajEc130_assertion description "[Missense mutations in the FVIII gene impairing the binding to VWF are a common cause of mild/moderate hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858348.RAW5bRaUVMLLaD7OrCIaJbEi3o5bijOqFZu6PRIFyajEc130_provenance.
- NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_assertion description "[Missense mutations in the FVIII gene impairing the binding to VWF are a common cause of mild/moderate hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392318.RAQ-K3dD7IdF0YtTrcH5XPwVgMc9qrMYQ10EL7hCkRARo130_provenance.
- NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_assertion description "[Missense mutations in the FVIII gene impairing the binding to VWF are a common cause of mild/moderate hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_provenance.