Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_provenance.
- NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_assertion description "[Considering the very large size of the USH2A gene and the high number of mutations detected in USH2 patients worldwide, our findings have significant implications for genetic counseling and carrier screening in various Jewish populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_provenance.
- NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_assertion evidence source_evidence_curated NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_provenance.
- NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_assertion SIO_000772 18452394 NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_provenance.
- NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_assertion wasDerivedFrom uniprot-2016 NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_provenance.
- NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_assertion wasGeneratedBy ECO_0000218 NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP5367.RAGXTHP928qanWz04RuJdeXmZyf0F6S-cKWCK0tT77CsQ130_provenance.