Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_provenance.
- NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_assertion description "[The polymorphic forms of 388 nucleotide of the OATP-2 gene were identified as risk factors for hyperbilirubinemia of unknown etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_provenance.
- NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_assertion evidence source_evidence_literature NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_provenance.
- NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_assertion SIO_000772 21500146 NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_provenance.
- NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_assertion wasDerivedFrom befree-2016 NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_provenance.
- NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_assertion wasGeneratedBy ECO_0000203 NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_provenance.
- befree-2016 importedOn "2016-02-19" NP887861.RArF_p8IHmngIE0GbD5ucedtFArG5FzeG4oVAxoPUO_WM130_provenance.