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- source_evidence_literature type ECO_0000212 NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_provenance.
- NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_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." NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_provenance.
- NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_assertion evidence source_evidence_literature NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_provenance.
- NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_assertion SIO_000772 23484049 NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_provenance.
- NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_assertion wasDerivedFrom befree-20150227 NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_provenance.
- NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_assertion wasGeneratedBy ECO_0000203 NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP740410.RAq0JJSWlD2ROsG-uW-M_82F8ZHPSGdGoNW0Y_7IGtDI4130_provenance.