Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_provenance.
- NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_assertion description "[Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_provenance.
- NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_assertion evidence source_evidence_literature NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_provenance.
- NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_assertion SIO_000772 20507940 NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_provenance.
- NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_assertion wasDerivedFrom befree-20150227 NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_provenance.
- NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_assertion wasGeneratedBy ECO_0000203 NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_provenance.