Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_provenance.
- NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_assertion wasGeneratedBy ECO_0000218 NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_provenance.
- NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_assertion wasDerivedFrom uniprot-20150221 NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_provenance.
- NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_assertion SIO_000772 8554073 NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_provenance.
- NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_assertion evidence source_evidence_curated NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_provenance.
- NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_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." NP2734.RAtW3RILHkfwI8P3bcixwwCPL8rn9hjAJ8UQ9ywBnMEOc130_provenance.