Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_provenance.
- NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_assertion description "[NPHS1 and NPHS2 gene mutations in Chinese children with sporadic nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_provenance.
- NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_assertion evidence source_evidence_literature NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_provenance.
- NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_assertion SIO_000772 17211152 NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_provenance.
- NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_assertion wasDerivedFrom befree-2016 NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_provenance.
- NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_assertion wasGeneratedBy ECO_0000203 NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_provenance.
- befree-2016 importedOn "2016-02-19" NP587864.RA2rdjve1duKuztq_wC5MY1d3QccX8toj-h1fJHKw6ydA130_provenance.