Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_provenance.
- NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_assertion description "[Three-locus AGT haplotype analysis (A-6G/T174M/M235T) identified DN-protective (ATM, AMM, GTM) and DN-susceptible (GTM, ATT, GMT and AMT) haplotypes, and demonstrated enrichment of GTT haplotype in macroalbuminuric compared to microalbuminuric or normoalbuminuric patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_provenance.
- NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_assertion evidence source_evidence_literature NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_provenance.
- NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_assertion SIO_000772 21421655 NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_provenance.
- NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_assertion wasDerivedFrom befree-20140225 NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_provenance.
- NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_assertion wasGeneratedBy ECO_0000203 NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP826115.RAF7SOU_BgMQUvLmSFncVnrWGqOYAqmIEhgjwc8-Owr7o130_provenance.