Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_provenance.
- NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_assertion description "[Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_provenance.
- NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_assertion evidence source_evidence_curated NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_provenance.
- NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_assertion SIO_000772 10802646 NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_provenance.
- NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_assertion wasDerivedFrom ctd_human-2016 NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_provenance.
- NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_assertion wasGeneratedBy ECO_0000218 NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP10758.RAOaL6S5qOygwl2L6QWnGYGlUNg967uAg7flH44zRxYIY130_provenance.