Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_provenance.
- NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_assertion description "[This discrepancy between observed (genotypic) and estimated (phenotypic) prevalence could be due to the existence of non-pathological or low penetrance alleles, which may result in late-onset arSTGD or may be implicated in age-related macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_provenance.
- NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_assertion evidence source_evidence_literature NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_provenance.
- NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_assertion SIO_000772 18977788 NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_provenance.
- NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_assertion wasDerivedFrom gad-20150221 NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_provenance.
- NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_assertion wasGeneratedBy ECO_0000203 NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP132506.RAQlHLT8DVSORIyR87qVEJMnP1Y2ME5GvdFGV3S-dh-Nk130_provenance.