Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_provenance.
- NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_assertion description "[A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_provenance.
- NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_assertion evidence source_evidence_literature NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_provenance.
- NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_assertion SIO_000772 10899453 NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_provenance.
- NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_assertion wasDerivedFrom befree-20150227 NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_provenance.
- NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_assertion wasGeneratedBy ECO_0000203 NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP720624.RAuM8HWi-UHde0GZDcynSKFKxhXkQWugSniJuHQaQVXNw130_provenance.