Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_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.
- 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.
- befree-20150227 importedOn "2015-02-27" NP741969.RAhpBwjvNzC98xZ90zLqCxvdqPy5prqkQGPvSMlCz5RZQ130_provenance.