Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_assertion> ?p ?o ?g. }
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- NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_assertion type Assertion NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_head.
- 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.
- NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_assertion evidence source_evidence_literature NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_provenance.
- NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_assertion SIO_000772 18385087 NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_provenance.
- NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_assertion wasDerivedFrom befree-20150227 NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_provenance.
- NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_assertion wasGeneratedBy ECO_0000203 NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_provenance.