Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_assertion type Assertion NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_head.
- NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_assertion wasGeneratedBy ECO_0000203 NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_provenance.
- NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_assertion wasDerivedFrom befree-2016 NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_provenance.
- NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_assertion SIO_000772 20370797 NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_provenance.
- NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_assertion evidence source_evidence_literature NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_provenance.
- NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_assertion description "[Genetic studies were performed to detect mutations in the SLC22A5 for primary carnitine deficiency, PNPLA2 for neutral lipid storage disease with myopathy, ABHD5 for neutral lipid storage disease with ichthyosis, ETFDH for multiple acyl-CoA dehydrogenation deficiency (MADD), and CPT2 for carnitine palmitoyltransferase II deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804313.RAKZwyDtTZ2x1fZZFIkhqSfSKhAcKjQvhHtWGn8dcqv6M130_provenance.