Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_provenance.
- NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_assertion description "[The metabolic role of malonyl CoA decarboxylase has not been fully defined, but deficiency of the enzyme has been associated with mild mental retardation, seizures, hypotonia, cardiomyopathy, vomiting, hypoglycemia, metabolic acidosis, and malonic aciduria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_provenance.
- NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_assertion evidence source_evidence_literature NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_provenance.
- NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_assertion SIO_000772 9869665 NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_provenance.
- NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_assertion wasDerivedFrom befree-2016 NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_provenance.
- NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_assertion wasGeneratedBy ECO_0000203 NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1411947.RA7WM15R9PTDr11z1V-1jNKCTpq7kH_I8LoP8-LaEpLcg130_provenance.