Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1117600.RAYnqMVQ82TkAK0M_V10VVqJwhFl6XtHLydqvMSQYvhMY130_provenance.