Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_provenance.
- NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_assertion wasGeneratedBy ECO_0000218 NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_provenance.
- NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_assertion wasDerivedFrom uniprot-2016 NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_provenance.
- NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_assertion SIO_000772 12696021 NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_provenance.
- NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_assertion evidence source_evidence_curated NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_provenance.
- NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_assertion description "[2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency is caused by mutations in the HADH2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_provenance.