Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_provenance.
- NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_assertion wasGeneratedBy ECO_0000218 NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_provenance.
- NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_assertion wasDerivedFrom uniprot-20150221 NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_provenance.
- NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_assertion SIO_000772 11349232 NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_provenance.
- NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_assertion evidence source_evidence_curated NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_provenance.
- NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_assertion description "[Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1503.RANEqLnQtnU701AprV6488v5HOJ7Ez6P1C_JPpSsh9DOg130_provenance.