Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_provenance.
- NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_assertion description "[Molecular survey of a prevalent mutation, 985A-to-G transition, and identification of five infrequent mutations in the medium-chain Acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_provenance.
- NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_assertion evidence source_evidence_literature NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_provenance.
- NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_assertion SIO_000772 1684086 NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_provenance.
- NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_assertion wasDerivedFrom befree-2016 NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_provenance.
- NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_assertion wasGeneratedBy ECO_0000203 NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_provenance.
- befree-2016 importedOn "2016-02-19" NP559737.RAy7PDke_Z3T2DJbBSSON3C4u5GdVj6DZfTPkVEGCc3vs130_provenance.