Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_assertion> ?p ?o ?g. }
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- NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_assertion type Assertion NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_head.
- NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_assertion description "[The genetic mutation underlying malonyl CoA decarboxylase deficiency was determined in a patient with clinical features of this defect, malonic aciduria, and markedly reduced malonyl CoA decarboxylase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_provenance.
- NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_assertion evidence source_evidence_literature NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_provenance.
- NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_assertion SIO_000772 9869665 NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_provenance.
- NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_assertion wasDerivedFrom befree-20140225 NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_provenance.
- NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_assertion wasGeneratedBy ECO_0000203 NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_provenance.