Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_provenance.
- NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_assertion description "[Cases showed a significantly higher frequency of FVL GA (OR = 21�38, P<0�0001) and FII GA (OR = 36�7, P<0�0001) genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_provenance.
- NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_assertion evidence source_evidence_literature NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_provenance.
- NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_assertion SIO_000772 21269570 NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_provenance.
- NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_assertion wasDerivedFrom befree-2016 NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_provenance.
- NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_assertion wasGeneratedBy ECO_0000203 NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_provenance.
- befree-2016 importedOn "2016-02-19" NP867926.RAH45pgAM1QJrFkfVAbMiar7b93gHoN79Bl92qlDNYNVk130_provenance.