Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_provenance.
- NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_assertion description "[Our results show a low prevalence of disease causing mutations in the NPHS1 (22% early onset, 5.5% overall) and NPHS2 (3.3% early onset and 3.4% overall) genes in the Pakistani NS children as compared to the European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_provenance.
- NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_assertion evidence source_evidence_literature NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_provenance.
- NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_assertion SIO_000772 22565185 NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_provenance.
- NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_assertion wasDerivedFrom befree-2016 NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_provenance.
- NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_assertion wasGeneratedBy ECO_0000203 NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_provenance.
- befree-2016 importedOn "2016-02-19" NP980276.RAc-5lRAp0k27au9QgJg0m3uC9iR_nJOfpfbOSGL69XLs130_provenance.