Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_assertion> ?p ?o ?g. }
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- NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_assertion type Assertion NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_head.
- NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_assertion wasGeneratedBy ECO_0000218 NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_provenance.
- NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_assertion wasDerivedFrom uniprot-2016 NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_provenance.
- NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_assertion SIO_000772 11349232 NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_provenance.
- NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_assertion evidence source_evidence_curated NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_provenance.
- NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_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." NP1407.RAt80S0sejyCABQJqLC0K_T-YxgIJk9I8Ri8koK7-JyMw130_provenance.