Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_provenance.
- NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_assertion description "[Mutations in the Stargardt disease gene (ABCR) were previously reported in patients with atrophic forms of AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_provenance.
- NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_assertion evidence source_evidence_literature NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_provenance.
- NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_assertion SIO_000772 10634626 NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_provenance.
- NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_assertion wasDerivedFrom befree-2016 NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_provenance.
- NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_assertion wasGeneratedBy ECO_0000203 NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_provenance.
- befree-2016 importedOn "2016-02-19" NP272455.RAtHf1K3HdAdPdXP-tFPb2QWIazOAKRkDsmWXEGb7DW-0130_provenance.