Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_assertion> ?p ?o ?g. }
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- NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_assertion type Assertion NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_head.
- NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_assertion wasGeneratedBy ECO_0000203 NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance.
- NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_assertion wasDerivedFrom befree-20140225 NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance.
- NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_assertion SIO_000772 9684781 NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance.
- NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_assertion evidence source_evidence_literature NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance.
- 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.