Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_provenance.
- NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_assertion description "[Recently, patients with early liver failure, renal tubulopathy and encephalopathy due to the mutations in the BCS1L gene coding for a structural protein in mitochondrial complex III have been described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_provenance.
- NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_assertion evidence source_evidence_literature NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_provenance.
- NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_assertion SIO_000772 23892085 NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_provenance.
- NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_assertion wasDerivedFrom befree-20150227 NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_provenance.
- NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_assertion wasGeneratedBy ECO_0000203 NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP265967.RA9Zgh5HKsycebFhRUW2nwdufzXW0snQ4BGHZVkuJjZR0130_provenance.