Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_provenance.
- NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_assertion description "[Mutation analysis of very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: identification and characterization of mutant VLCAD cDNAs from four patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_provenance.
- NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_assertion evidence source_evidence_curated NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_provenance.
- NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_assertion SIO_000772 8554073 NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_provenance.
- NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_assertion wasDerivedFrom uniprot-20130724 NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_provenance.
- NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_assertion wasGeneratedBy ECO_0000218 NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP130.RAzMrqr_OcURZUU6wsYa1poheiHrb1Tlh8I5Ch4BM5YIo130_provenance.