Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_provenance.
- NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_assertion description "[Depending on the clinical and biochemical phenotype we suggest POLG1, SUCLA2, TMEM70 and RYR1 sequence analysis and mtDNA-depletion studies in children with 3-methylglutaconic aciduria type IV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_provenance.
- NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_assertion evidence source_evidence_literature NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_provenance.
- NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_assertion SIO_000772 19015156 NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_provenance.
- NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_assertion wasDerivedFrom befree-2016 NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_provenance.
- NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_assertion wasGeneratedBy ECO_0000203 NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_provenance.
- befree-2016 importedOn "2016-02-19" NP704009.RA0Qyi2i3NK53M9F7gNIRGIqR4JLj56iAIWmx4qh4HYd0130_provenance.