Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_provenance.
- NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_assertion description "[Furthermore, the frequency of LVH in hypertensives was significantly higher in the subjects with both the BDKRB2 CC and ACE D allele than those with other genotypes (p =0.002, chi2 =9.4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_provenance.
- NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_assertion evidence source_evidence_literature NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_provenance.
- NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_assertion SIO_000772 15894833 NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_provenance.
- NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_assertion wasDerivedFrom befree-2016 NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_provenance.
- NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_assertion wasGeneratedBy ECO_0000203 NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP494868.RAxiqEIfWxmIyedY2ezsFWsoUFRSjCt_VaUhd0Gx5oHmQ130_provenance.