Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_assertion> ?p ?o ?g. }
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- NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_assertion type Assertion NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_head.
- NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_assertion description "[The defective FVIII carrier function of von Willebrand factor (VWF) identifies type 2N von Willebrand disease (VWD), a variant with a pattern resembling hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_provenance.
- NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_assertion evidence source_evidence_literature NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_provenance.
- NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_assertion SIO_000772 17456630 NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_provenance.
- NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_assertion wasDerivedFrom befree-20140225 NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_provenance.
- NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_assertion wasGeneratedBy ECO_0000203 NP224462.RAgMb-wvKJPq4eWdMttgEWuBiXCjYfh92oGBWgabadBqM130_provenance.