Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_assertion> ?p ?o ?g. }
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- NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_assertion type Assertion NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_head.
- NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_assertion wasGeneratedBy ECO_0000218 NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_provenance.
- NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_assertion wasDerivedFrom uniprot-20130724 NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_provenance.
- NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_assertion SIO_000772 11349232 NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_provenance.
- NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_assertion evidence source_evidence_curated NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_provenance.
- NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_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." NP121.RATCV9AIYHvRU3J0rci94FrrQWuv5mFuH81u73A7NbmRE130_provenance.