Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_assertion> ?p ?o ?g. }
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- NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_assertion type Assertion NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_head.
- NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_assertion wasGeneratedBy ECO_0000203 NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_provenance.
- NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_assertion wasDerivedFrom befree-20150227 NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_provenance.
- NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_assertion SIO_000772 11952089 NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_provenance.
- NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_assertion evidence source_evidence_literature NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_provenance.
- NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_assertion description "[A variety of mutations found in GCAP and retGC genes have been linked to several forms of human congenital retinal diseases, such as dominant cone degeneration, cone-rod dystrophy and Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441902.RABM4Y2ZRAra_rw2I9caCRmbbZmxUEeXU_dFEKhzJTImc130_provenance.