Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_assertion> ?p ?o ?g. }
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- NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_assertion type Assertion NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_head.
- 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.
- NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_assertion evidence source_evidence_literature NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_provenance.
- NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_assertion SIO_000772 18184946 NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_provenance.
- NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_assertion wasDerivedFrom befree-20140225 NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_provenance.
- NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_assertion wasGeneratedBy ECO_0000203 NP676003.RALNLUVDuTdBu8-hEecOGQVwE3-TDn-p0Kz5QsLn4mAAU130_provenance.