Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_provenance.
- NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_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." NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_provenance.
- NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_assertion evidence source_evidence_curated NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_provenance.
- NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_assertion SIO_000772 12696021 NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_provenance.
- NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_assertion wasDerivedFrom uniprot-20130724 NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_provenance.
- NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_assertion wasGeneratedBy ECO_0000218 NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3134.RAS_nqKGah979DxrXvZE-DOZE9IwRR25I8C93bF47IwIg130_provenance.