Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_provenance.
- NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_assertion description "[In two independent patients with classical xanthinuria type II, we identified a C to T base substitution at nucleotide 1255 in the HMCS gene that should cause a CGA (Arg) to TGA (Ter) nonsense substitution at codon 419.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_provenance.
- NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_assertion evidence source_evidence_literature NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_provenance.
- NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_assertion SIO_000772 11302742 NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_provenance.
- NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_assertion wasDerivedFrom befree-2016 NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_provenance.
- NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_assertion wasGeneratedBy ECO_0000203 NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_provenance.
- befree-2016 importedOn "2016-02-19" NP314389.RA8MKRb2IqIkiJKfhQatHktUoWM9sj086-uhySFXR6EnM130_provenance.