Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_provenance.
- NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_assertion description "[All of our patients carried autosomal recessive mutations in ETFDH, suggesting that ETFDH deficiency leads to a secondary CoQ10 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_provenance.
- NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_assertion evidence source_evidence_literature NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_provenance.
- NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_assertion SIO_000772 17412732 NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_provenance.
- NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_assertion wasDerivedFrom befree-20140225 NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_provenance.
- NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_assertion wasGeneratedBy ECO_0000203 NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP921966.RA22KbIvtFEMp5o8xiLSQF46iUSC5v4x_k613o-KA4hUo130_provenance.