Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_provenance.
- NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_assertion description "[Further genotype pattern frequency analysis in TLR-2 SNPs (rs3804099 and rs3804100) showed significantly reduced occurrence of the rare allele homozygote (CC+CC) in the no-VUR subgroup of APN and ALN cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_provenance.
- NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_assertion evidence source_evidence_literature NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_provenance.
- NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_assertion SIO_000772 23484049 NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_provenance.
- NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_assertion wasDerivedFrom befree-20150227 NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_provenance.
- NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_assertion wasGeneratedBy ECO_0000203 NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP740538.RAqW7UaE7n9PGa0S1ZlXtFWfW418GydFBPQ5mLwvHlUuk130_provenance.