Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_provenance.
- NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_assertion description "[Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_provenance.
- NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_assertion evidence source_evidence_literature NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_provenance.
- NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_assertion SIO_000772 14623864 NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_provenance.
- NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_assertion wasDerivedFrom befree-2016 NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_provenance.
- NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_assertion wasGeneratedBy ECO_0000203 NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_provenance.
- befree-2016 importedOn "2016-02-19" NP420986.RAFn1Gs9wcPKAaq6DU0ldKKJV4wT6U49Neu21SXUccEEo130_provenance.