Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_provenance.
- NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_assertion description "[Two haplotypes were associated with increased risk of primary DCM: DRB1*0401/DQB1*0302 (OR = 4.53, P = 0.002) and DRB1*0401/DQB1*0401 (OR = 9.42, P = 0.004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_provenance.
- NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_assertion evidence source_evidence_literature NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_provenance.
- NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_assertion SIO_000772 20136773 NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_provenance.
- NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_assertion wasDerivedFrom befree-2016 NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_provenance.
- NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_assertion wasGeneratedBy ECO_0000203 NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_provenance.
- befree-2016 importedOn "2016-02-19" NP792176.RAVPQf72Y-nbdlS-C2eWLLAsMLIPZKfq0WMSOZlqgbPoc130_provenance.