Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_provenance.
- NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_assertion description "[Subjects with CHC carrying DDX5 minor allele or DDX5-POLG2 haplotypes are at an increased risk of developing advanced fibrosis, whereas those carrying the CPT1A minor allele are at a decreased risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_provenance.
- NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_assertion evidence source_evidence_literature NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_provenance.
- NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_assertion SIO_000772 16697732 NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_provenance.
- NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_assertion wasDerivedFrom gad-20150221 NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_provenance.
- NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_assertion wasGeneratedBy ECO_0000203 NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP100566.RAhP0jdXn6j6G8LgED7WTyomN41xahavZXkbTnPHubxLk130_provenance.