Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_provenance.
- NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_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." NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_provenance.
- NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_assertion evidence source_evidence_literature NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_provenance.
- NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_assertion SIO_000772 16697732 NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_provenance.
- NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_assertion wasDerivedFrom befree-20140225 NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_provenance.
- NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_assertion wasGeneratedBy ECO_0000203 NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP458228.RA2nIWVs2jBH7LOKNLc87EG_EEoiqxto5kIjm3QAAC1O4130_provenance.