Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_provenance.
- NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_assertion description "[Our data suggest that an inborn error (i.e., high Km of transketolase for thiamine pyrophosphate) predisposing to thiamine deficiency diseases similar to those reported in Wernicke-Korsakoff syndrome may occur in the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_provenance.
- NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_assertion evidence source_evidence_literature NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_provenance.
- NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_assertion SIO_000772 3558815 NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_provenance.
- NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_assertion wasDerivedFrom befree-20150227 NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_provenance.
- NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_assertion wasGeneratedBy ECO_0000203 NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP739612.RARdFS6MEptsDU--E3Bhsw-1r1xTTrkih32A8C5lA4ULc130_provenance.