Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_provenance.
- NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_assertion description "[The affected boy, who possesses mutant HSD10 (p.V65A), has a neurological syndrome with metabolic derangements, choreoathetosis, refractory epilepsy and learning disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_provenance.
- NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_assertion evidence source_evidence_literature NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_provenance.
- NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_assertion SIO_000772 22132097 NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_provenance.
- NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_assertion wasDerivedFrom befree-2016 NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_provenance.
- NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_assertion wasGeneratedBy ECO_0000203 NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP943146.RAVybd_p2m1X4I7k9k4yCyyCZqg0OI4lTwE0q6M_fhEsQ130_provenance.