Matches in Nanopublications for { ?s ?p "[Extensive laboratory investigations indicate that the short-chain acyl-CoA dehydrogenase gene variant is likely preventing or delaying the normal expression of the Prader-Willi syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Extensive laboratory investigations indicate that the short-chain acyl-CoA dehydrogenase gene variant is likely preventing or delaying the normal expression of the Prader-Willi syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP120278.RAncwRIaD8itZJHFYT5bb90TJCQgLaJ7Is1kI66Wgt-X0130_assertion description "[Extensive laboratory investigations indicate that the short-chain acyl-CoA dehydrogenase gene variant is likely preventing or delaying the normal expression of the Prader-Willi syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120278.RAncwRIaD8itZJHFYT5bb90TJCQgLaJ7Is1kI66Wgt-X0130_provenance.
- NP233144.RAQSPuaBk8_uASsbuAXjAgL-nodXd8QqdI7ALrUPM18tc130_assertion description "[Extensive laboratory investigations indicate that the short-chain acyl-CoA dehydrogenase gene variant is likely preventing or delaying the normal expression of the Prader-Willi syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233144.RAQSPuaBk8_uASsbuAXjAgL-nodXd8QqdI7ALrUPM18tc130_provenance.
- NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_assertion description "[Extensive laboratory investigations indicate that the short-chain acyl-CoA dehydrogenase gene variant is likely preventing or delaying the normal expression of the Prader-Willi syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_provenance.
- NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_assertion description "[Extensive laboratory investigations indicate that the short-chain acyl-CoA dehydrogenase gene variant is likely preventing or delaying the normal expression of the Prader-Willi syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_provenance.