Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_assertion type Assertion NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_head.
- NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_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." NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_provenance.
- NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_assertion evidence source_evidence_literature NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_provenance.
- NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_assertion SIO_000772 19563498 NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_provenance.
- NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_assertion wasDerivedFrom befree-20140225 NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_provenance.
- NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_assertion wasGeneratedBy ECO_0000203 NP162460.RAcry1lm0SJUBcNVfwAZRte6ioAYTFGNUXsupAJFnCeBI130_provenance.