Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- 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.
- 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." provenance.
- NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_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." NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_provenance.
- NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_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." NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_provenance.