Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_provenance.
- NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_assertion description "[FSGS1 may have widely variable clinical and pathological phenotypes and therefore should be considered in young children with full-blown and rapidly progressing nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_provenance.
- NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_assertion evidence source_evidence_literature NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_provenance.
- NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_assertion SIO_000772 18436095 NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_provenance.
- NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_assertion wasDerivedFrom befree-2016 NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_provenance.
- NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_assertion wasGeneratedBy ECO_0000203 NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_provenance.
- befree-2016 importedOn "2016-02-19" NP667756.RAiXm2rHYBBIG6eslIJNeRPunbWgLP1cJeVKpQXT4k_4w130_provenance.