Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_provenance.
- NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_assertion description "[The purpose of this study was to determine the prevalence of mutations in the peripherin/RDS gene in Spanish patients with different types of autosomal dominant macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_provenance.
- NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_assertion evidence source_evidence_literature NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_provenance.
- NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_assertion SIO_000772 17653047 NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_provenance.
- NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_assertion wasDerivedFrom befree-2016 NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_provenance.
- NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_assertion wasGeneratedBy ECO_0000203 NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_provenance.
- befree-2016 importedOn "2016-02-19" NP621712.RAdOSFuJeeGChAK9nxomebR5nq56DiaASC1mXDaDEck_g130_provenance.