Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_provenance.
- NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_assertion description "[These results suggested that CTLA-4 +49 A/G polymorphism does not contribute to susceptibility to HSP; however, the presence of CTLA-4 AG genotype and HLA-DRB1*13 could be a risk factor for developing nephrotic-range proteinuria in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_provenance.
- NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_assertion evidence source_evidence_literature NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_provenance.
- NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_assertion SIO_000772 18449568 NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_provenance.
- NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_assertion wasDerivedFrom befree-20150227 NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_provenance.
- NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_assertion wasGeneratedBy ECO_0000203 NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP455873.RA-vlnwdM8SN8dgMz1VesFgz7tcCtNDxhSb6y0_dIRPb4130_provenance.