Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_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.
- NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_assertion evidence source_evidence_literature NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_provenance.
- NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_assertion SIO_000772 18385087 NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_provenance.
- NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_assertion wasDerivedFrom befree-2016 NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_provenance.
- NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_assertion wasGeneratedBy ECO_0000203 NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_provenance.
- befree-2016 importedOn "2016-02-19" NP663745.RAm2Vf3dHK254zSBgE_0kUvkb_7qiUf_aLDJr8Z_pul0M130_provenance.