Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_provenance.
- NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_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." NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_provenance.
- NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_assertion evidence source_evidence_curated NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_provenance.
- NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_assertion SIO_000772 19793595 NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_provenance.
- NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_assertion wasDerivedFrom ctd_human-20150221 NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_provenance.
- NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_assertion wasGeneratedBy ECO_0000218 NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP21105.RANOgjz3eL25-wwlg9GKL-WlB8RD1g1gJB8PRK69YkrYI130_provenance.