Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_provenance.
- NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_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." NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_provenance.
- NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_assertion evidence source_evidence_literature NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_provenance.
- NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_assertion SIO_000772 23975748 NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_provenance.
- NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_assertion wasDerivedFrom befree-2016 NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_provenance.
- NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_assertion wasGeneratedBy ECO_0000203 NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1105237.RAflGbrjKVs80gs29Ux2exH2q_y9JKzwvGahvpa5diYFA130_provenance.