Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_assertion> ?p ?o ?g. }
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- NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_assertion type Assertion NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_head.
- NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_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." NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_provenance.
- NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_assertion evidence source_evidence_literature NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_provenance.
- NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_assertion SIO_000772 23484049 NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_provenance.
- NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_assertion wasDerivedFrom befree-2016 NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_provenance.
- NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_assertion wasGeneratedBy ECO_0000203 NP1059865.RAl_tXyWXZwoA9kv8t3IGZ3luJ7umLDP--PuC6548qF_4130_provenance.