Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_assertion type Assertion NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_head.
- NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_assertion description "[Nevertheless, the mutations p.Asp845Glu, p.Pro947Arg, p.Glu1057Lys, p.His1066Tyr, p.Arg1126Trp, p.Arg1329His, p.Leu1481Pro, and p.Ala1610Ser resulted in decreased FVIII:C values that may explain mild HA phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_provenance.
- NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_assertion evidence source_evidence_literature NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_provenance.
- NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_assertion SIO_000772 24108539 NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_provenance.
- NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_assertion wasDerivedFrom befree-2016 NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_provenance.
- NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_assertion wasGeneratedBy ECO_0000203 NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_provenance.