Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_provenance.
- NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_assertion description "[All 8 exons of NPHS2 were sequenced in 99 children, including 49 with SRNS and 50 with steroid-sensitive nephrotic syndrome (control group) by DNA sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_provenance.
- NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_assertion evidence source_evidence_literature NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_provenance.
- NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_assertion SIO_000772 24072147 NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_provenance.
- NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_assertion wasDerivedFrom befree-2016 NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_provenance.
- NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_assertion wasGeneratedBy ECO_0000203 NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1114088.RAPkZrEV7q4SGfpsi0DnPiIX3oksDroPDn1KqQ-TgOGS4130_provenance.