Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_provenance.
- NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_assertion description "[Mutations in the peripherin/retinal degeneration slow (RDS) gene have been identified in patients with retinitis pigmentosa and pattern macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_provenance.
- NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_assertion evidence source_evidence_literature NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_provenance.
- NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_assertion SIO_000772 7862413 NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_provenance.
- NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_assertion wasDerivedFrom befree-2016 NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_provenance.
- NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_assertion wasGeneratedBy ECO_0000203 NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1324178.RAP1enC00y8-tHsJIRY0H8fubrf_HZwsVPeIeIwX5QxKM130_provenance.