Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_provenance.
- NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_assertion description "[Nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase (complex I) enzyme deficiencies account for a significant proportion of mitochondrial disorders, including LS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_provenance.
- NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_assertion evidence source_evidence_literature NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_provenance.
- NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_assertion SIO_000772 23266820 NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_provenance.
- NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_assertion wasDerivedFrom befree-20150227 NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_provenance.
- NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_assertion wasGeneratedBy ECO_0000203 NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP800005.RAjHVmFUTtpiXWo1c3m54C06CFQWvSAsUg_jNYGctupDQ130_provenance.