Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion description "[Three of the patients were homozygous for the 'common' 1528G>C mutation in the alpha-subunit of the MTP, giving rise to long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion evidence source_evidence_literature NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion SIO_000772 14605499 NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion wasDerivedFrom befree-20140225 NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion wasGeneratedBy ECO_0000203 NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.