Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_provenance.
- NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_assertion description "[A population-attributable risk of approximately 50% for the Pro12Pro genotype indicates that testing for the Pro12Ala of the PPARG gene in addition to the already identified clinical risk factors may become a useful tool to further reduce the risk of PPAR]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_provenance.
- NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_assertion evidence source_evidence_literature NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_provenance.
- NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_assertion SIO_000772 16822823 NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_provenance.
- NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_assertion wasDerivedFrom gad-20150221 NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_provenance.
- NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_assertion wasGeneratedBy ECO_0000203 NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP101472.RAVz3OjcDjcLdX-4Tci7KV_mOsT-ZJ8CQFNpN5txRN9Aw130_provenance.