Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_provenance.
- NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_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." NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_provenance.
- NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_assertion evidence source_evidence_literature NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_provenance.
- NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_assertion SIO_000772 20507940 NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_provenance.
- NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_assertion wasDerivedFrom befree-2016 NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_provenance.
- NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_assertion wasGeneratedBy ECO_0000203 NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_provenance.
- befree-2016 importedOn "2016-02-19" NP815298.RAtiGxlK9RBWx9MSpE6pG8cp-qADhEBif2yL7eT9LETGc130_provenance.