Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_assertion> ?p ?o ?g. }
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- NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_assertion type Assertion NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_head.
- NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_assertion description "[A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_provenance.
- NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_assertion evidence source_evidence_curated NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_provenance.
- NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_assertion SIO_000772 22565185 NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_provenance.
- NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_assertion wasDerivedFrom uniprot-2016 NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_provenance.
- NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_assertion wasGeneratedBy ECO_0000218 NP7078.RA1MHg3jSrPWgHBMgpFto4EiHeP3op474P0Wr_LFGn7vA130_provenance.