Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_assertion> ?p ?o ?g. }
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- NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_assertion type Assertion NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_head.
- NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_assertion wasGeneratedBy ECO_0000218 NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_provenance.
- NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_assertion wasDerivedFrom uniprot-2016 NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_provenance.
- NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_assertion SIO_000772 8088787 NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_provenance.
- NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_assertion evidence source_evidence_curated NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_provenance.
- NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_assertion description "[Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8728.RADC8MvMsSpeg7N2soAfpcPCtZOuSK9yURbFrdJm-X8Pc130_provenance.