Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_assertion> ?p ?o ?g. }
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- NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_assertion type Assertion NP597429.RATfI8Qb_1hdIq39fSo327XfMX1fg7DzZNe0TaaOmfJpI130_head.
- 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.