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- source_evidence_literature type ECO_0000212 NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_provenance.
- NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_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." NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_provenance.
- NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_assertion evidence source_evidence_literature NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_provenance.
- NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_assertion SIO_000772 18385087 NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_provenance.
- NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_assertion wasDerivedFrom gad-20130706 NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_provenance.
- NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_assertion wasGeneratedBy ECO_0000203 NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_provenance.
- gad-20130706 importedOn "2013-07-06" NP50367.RAQW58-M095D0hMQWP-V6CJloGwGT1Ms8HoOCcvvGXi7o130_provenance.