Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP694241.RANtRBRh7CxROO4hEHCY68xCPx1qPBWoQNQ1qRxmCWAXM130_provenance.