Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_assertion> ?p ?o ?g. }
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- NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_assertion type Assertion NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_head.
- NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_assertion description "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_provenance.
- NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_assertion evidence source_evidence_curated NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_provenance.
- NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_assertion SIO_000772 20956273 NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_provenance.
- NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_assertion wasDerivedFrom uniprot-2016 NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_provenance.
- NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_assertion wasGeneratedBy ECO_0000218 NP6398.RATvXGBIUubklgcg0dNdQV6ClFFfoCdMotmJuP6R6c-aM130_provenance.