Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_provenance.
- NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_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." NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_provenance.
- NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_assertion evidence source_evidence_literature NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_provenance.
- NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_assertion SIO_000772 23484049 NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_provenance.
- NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_assertion wasDerivedFrom befree-20140225 NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_provenance.
- NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_assertion wasGeneratedBy ECO_0000203 NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP420207.RAsiKHllnAkLERYy1SAk_KWicoLSCVzgqChavgNgUTfTI130_provenance.