Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_assertion> ?p ?o ?g. }
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- NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_assertion type Assertion NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_head.
- NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_assertion description "[Three distinct candidate point mutations of the von Willebrand factor gene in four patients with type IIA von Willebrand disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_provenance.
- NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_assertion evidence source_evidence_literature NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_provenance.
- NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_assertion SIO_000772 1380739 NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_provenance.
- NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_assertion wasDerivedFrom befree-2016 NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_provenance.
- NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_assertion wasGeneratedBy ECO_0000203 NP412614.RADC-npQp0uWMVh1a1Zvp8LR11kXZ2F6P22MW0SDWX7p4130_provenance.