Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_provenance.
- NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_assertion description "[Although an intronic SNP in TLR4 was associated marginally with AMD (P = 0.03), it was not possible to replicate a previous association with the rare coding SNP D299G in this gene (P = 0.6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_provenance.
- NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_assertion evidence source_evidence_literature NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_provenance.
- NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_assertion SIO_000772 18385087 NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_provenance.
- NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_assertion wasDerivedFrom befree-20140225 NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_provenance.
- NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_assertion wasGeneratedBy ECO_0000203 NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP438221.RADs3UqJsjLU5vRUkK7Hep4s-h5DVyxSoNrltwog2HshM130_provenance.