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- source_evidence_literature type ECO_0000212 NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_provenance.
- NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_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." NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_provenance.
- NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_assertion evidence source_evidence_literature NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_provenance.
- NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_assertion SIO_000772 23975748 NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_provenance.
- NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_assertion wasDerivedFrom befree-2016 NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_provenance.
- NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_assertion wasGeneratedBy ECO_0000203 NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_provenance.
- befree-2016 importedOn "2016-02-19" NP1105233.RAUmQT8BN20duMrLzkXXFTRwd_NwrGbQXcH7ag00LLN9A130_provenance.