Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_provenance.
- NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_assertion description "[Curiously, although the index patient inherited both Bernard Soulier syndrome and factor XI deficiency (FXI: C = 1.3%), he had mild bleeding symptoms restricted only to ecchymoses and petechiae.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_provenance.
- NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_assertion evidence source_evidence_literature NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_provenance.
- NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_assertion SIO_000772 15823864 NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_provenance.
- NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_assertion wasDerivedFrom befree-20150227 NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_provenance.
- NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_assertion wasGeneratedBy ECO_0000203 NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP392793.RAzJDaR1O1S83kvq28g2HiM-O-q93_tGWq52gHsuvxWlQ130_provenance.