Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_assertion> ?p ?o ?g. }
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- NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_assertion type Assertion NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_head.
- NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_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." NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_provenance.
- NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_assertion evidence source_evidence_literature NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_provenance.
- NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_assertion SIO_000772 23484049 NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_provenance.
- NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_assertion wasDerivedFrom befree-20140225 NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_provenance.
- NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_assertion wasGeneratedBy ECO_0000203 NP316766.RAwYPoXmE_pYTtTWFnKN_fHz2QrstTnLl_66pSH0axC3M130_provenance.