Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion> ?p ?o ?g. }
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- NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion type Assertion NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_head.
- NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion description "[von Willebrand disease (VWD) type 3 is a rare disorder characterized by absent or <0.1 UmL(-1) of ristocetin cofactor (VWF:RCo), and a very low level of factor VIII (FVIII:C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion evidence source_evidence_literature NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion SIO_000772 19563498 NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion wasDerivedFrom befree-20150227 NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.
- NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_assertion wasGeneratedBy ECO_0000203 NP323231.RAFVjeGX8nBFFG8UCVbFieD2DITQyF9M5bVHMSiZPmXD0130_provenance.