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- source_evidence_literature type ECO_0000212 NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_provenance.
- NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_assertion description "[In south Indian (SI) subjects there was significant allelic and genotypic association of the wild-type allele in SOD2 (Ala9Val; P=.002 and P=.013, respectively), UCP1 (-112 T>G, P=.012 and P=.009; Ala64Thr, P=.015 and P=.004), NOS3 (Glu298Asp, P=.002 and P=.009) and GSTP1 (Ile105Val, P=.003 and P=.004) genes with development of CRI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_provenance.
- NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_assertion evidence source_evidence_literature NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_provenance.
- NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_assertion SIO_000772 18413200 NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_provenance.
- NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_assertion wasDerivedFrom befree-20140225 NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_provenance.
- NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_assertion wasGeneratedBy ECO_0000203 NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP785978.RAsH2Iz-9GfgisnIlhB8wnxwZmOL3nSg_WfMsw6uecT_E130_provenance.