Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_provenance.
- NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_assertion description "[Hence, GLUD1 mutational analysis may be indicated in patients with leucine sensitivity; even in the absence of HA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_provenance.
- NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_assertion evidence source_evidence_literature NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_provenance.
- NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_assertion SIO_000772 19690084 NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_provenance.
- NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_assertion wasDerivedFrom befree-2016 NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_provenance.
- NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_assertion wasGeneratedBy ECO_0000203 NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_provenance.
- befree-2016 importedOn "2016-02-19" NP758224.RAs6EEV8bMIbSqCglfuEuf2_lR0ZTjh6y-QS-6B8ms5IA130_provenance.