Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_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.
- NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_assertion evidence source_evidence_literature NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_provenance.
- NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_assertion SIO_000772 18184946 NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_provenance.
- NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_assertion wasDerivedFrom lhgdn-20090331 NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_provenance.
- NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_assertion wasGeneratedBy ECO_0000203 NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP183471.RA8qpBpCOnSyVwcm2gB8aEJMwxyIHOgVrsRnSNYsMNMvM130_provenance.