Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_assertion> ?p ?o ?g. }
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- NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_assertion type Assertion NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_head.
- NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_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." NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_provenance.
- NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_assertion evidence source_evidence_literature NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_provenance.
- NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_assertion SIO_000772 20507940 NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_provenance.
- NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_assertion wasDerivedFrom befree-20140225 NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_provenance.
- NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_assertion wasGeneratedBy ECO_0000203 NP294592.RAl3NWqiURZ52jj_vngaByANAgQbnunB-iMRjM1SyCrlw130_provenance.