Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_provenance.
- NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_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." NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_provenance.
- NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_assertion evidence source_evidence_literature NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_provenance.
- NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_assertion SIO_000772 18413200 NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_provenance.
- NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_assertion wasDerivedFrom befree-20150227 NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_provenance.
- NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_assertion wasGeneratedBy ECO_0000203 NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP594403.RA5Nqkbg1vAcTWU-CjfUV0lThHNgRwVNwUWzn-XKrT3mg130_provenance.