Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_provenance.
- NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_assertion description "[Tandem mass spectrometry detected multiple acyl-CoA deficiency, leading to the analysis of the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene, previously shown to result in another metabolic disorder, glutaric aciduria type II (GAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_provenance.
- NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_assertion evidence source_evidence_literature NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_provenance.
- NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_assertion SIO_000772 17412732 NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_provenance.
- NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_assertion wasDerivedFrom befree-2016 NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_provenance.
- NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_assertion wasGeneratedBy ECO_0000203 NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_provenance.
- befree-2016 importedOn "2016-02-19" NP603093.RA4URAqWEqpNMiKr-xmhRVgZkblBO-WlzKWUvh6_3LdKA130_provenance.