Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_provenance.
- NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_assertion description "[However, significant association was identified for the CFHR3-1 deletion in AMD cases (p = 2.38 � 10(-12)) OR = 0.31, CI-0.95 (0.23-0.44), for both neovascular disease (nAMD) (p = 8.3 � 10(-9)) OR = 0.36 CI-0.95 (0.25-0.52) and geographic atrophy (GA) (p = 1.5 � 10(-6)) OR = 0.36 CI-0.95 (0.25-0.52) compared to controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_provenance.
- NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_assertion evidence source_evidence_literature NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_provenance.
- NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_assertion SIO_000772 22558131 NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_provenance.
- NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_assertion wasDerivedFrom befree-2016 NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_provenance.
- NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_assertion wasGeneratedBy ECO_0000203 NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_provenance.
- befree-2016 importedOn "2016-02-19" NP979656.RAckTtxym_cBiYcwVN5KAekq6OUzenv2cw7EW-rwqS8fI130_provenance.