Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_assertion type Assertion NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_head.
- NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_assertion description "[Mutations in the ACTN4 gene cause focal segmental glomerulosclerosis (FSGS), which shows autosomal dominant inheritance (Online Mendelian Inheritance in Man No.603278, FSGS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_provenance.
- NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_assertion evidence source_evidence_curated NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_provenance.
- NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_assertion SIO_000772 18436095 NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_provenance.
- NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_assertion wasDerivedFrom uniprot-2016 NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_provenance.
- NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_assertion wasGeneratedBy ECO_0000218 NP5358.RAiJExQrcSFJlj9ty_I_q6PLxpezdKgy7_exOdPI_MLwA130_provenance.