Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance.