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- source_evidence_literature type ECO_0000212 NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_provenance.
- NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_assertion description "[The +49GG genotype of the +49A/G SNP in the CTLA-4 gene is associated with the risk for MCD, FSGS and MN, suggesting a possible role for CTLA-4 in a proposed common final pathway in the pathogenesis of primary nephrotic kidney diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_provenance.
- NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_assertion evidence source_evidence_literature NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_provenance.
- NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_assertion SIO_000772 23975748 NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_provenance.
- NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_assertion wasDerivedFrom befree-20150227 NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_provenance.
- NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_assertion wasGeneratedBy ECO_0000203 NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP335349.RAD14ei_porFSjsKkOxOVr_nepyCtkOSirX0YAitLx1A4130_provenance.