Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_provenance.
- NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_assertion description "[Sequencing of candidate genes LMNA, PPARG, AKT2, caveolin-1, as well as the PPARG4 promoter gene, which are known to be associated with familial partial lipodystrophy, revealed no genetic abnormalities, suggesting that this case may involve a novel gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_provenance.
- NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_assertion evidence source_evidence_curated NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_provenance.
- NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_assertion SIO_000772 19793595 NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_provenance.
- NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_assertion wasDerivedFrom ctd_human-20130708 NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_provenance.
- NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_assertion wasGeneratedBy ECO_0000218 NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP26939.RAE03N4-XHJqFA878C1cKv5sxrQsRq3uf30_WXnavFN38130_provenance.