Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_provenance.
- NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_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." NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_provenance.
- NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_assertion evidence source_evidence_literature NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_provenance.
- NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_assertion SIO_000772 9869665 NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_provenance.
- NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_assertion wasDerivedFrom befree-20140225 NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_provenance.
- NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_assertion wasGeneratedBy ECO_0000203 NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP251955.RAk1OpoE0QhhQGh61PN0E5ZfSo5dtMlg6rJZ5Yu8wU3hE130_provenance.