Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_provenance.
- NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_assertion description "[Our goal was to study the occurrence of the SNPs -318C/T, +49A/G and CT60 on the CTLA-4 gene in healthy blood donors (N = 156) compared with nephrotic patients with biopsy-proven minimal-change disease (MCD, N = 160), focal segmental glomerulosclerosis (FSGS, N = 159) and membranous nephropathy (MN, N = 185).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_provenance.
- NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_assertion evidence source_evidence_literature NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_provenance.
- NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_assertion SIO_000772 23975748 NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_provenance.
- NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_assertion wasDerivedFrom befree-20150227 NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_provenance.
- NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_assertion wasGeneratedBy ECO_0000203 NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP987153.RA2IiS2xIKqDFQa8W5cc-byMCifPMPa5tFe1QckO0fh8M130_provenance.