Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_assertion type Assertion NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_head.
- NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_assertion description "[In five IC (15%), two mutant VWF alleles were not identified to explain the type 3 VWD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_provenance.
- NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_assertion evidence source_evidence_literature NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_provenance.
- NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_assertion SIO_000772 23311757 NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_provenance.
- NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_assertion wasDerivedFrom befree-2016 NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_provenance.
- NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_assertion wasGeneratedBy ECO_0000203 NP1042935.RAW_Ku42MRn-n1DWgA5Vx7XMRFcIcjjGxU-vkssTzIg70130_provenance.