Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_assertion> ?p ?o ?g. }
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- NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_assertion type Assertion NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_head.
- NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_assertion wasGeneratedBy ECO_0000203 NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_provenance.
- NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_assertion wasDerivedFrom befree-20140225 NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_provenance.
- NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_assertion SIO_000772 9684781 NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_provenance.
- NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_assertion evidence source_evidence_literature NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_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.