Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_assertion> ?p ?o ?g. }
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- NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_assertion type Assertion NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_head.
- NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_assertion wasGeneratedBy ECO_0000218 NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_provenance.
- NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_assertion wasDerivedFrom uniprot-20130724 NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_provenance.
- NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_assertion SIO_000772 11726550 NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_provenance.
- NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_assertion evidence source_evidence_curated NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_provenance.
- NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_assertion description "[Congenital nephrotic syndrome of the Finnish type (CNF or NPHS1) is an autosomal recessive kidney disorder resulting in severe proteinurea and renal dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4573.RATKFzVOLSUZsJDc4-YDuuGIVSRqUJXQCijZw8gl9by3A130_provenance.