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- NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_assertion type Assertion NP2633.RAilJPKTFliphdc125u25lsbjpNidDjN67hDlIIY15nnE130_head.
- 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.