Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_assertion> ?p ?o ?g. }
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- NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_assertion type Assertion NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_head.
- NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_assertion wasGeneratedBy ECO_0000203 NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_provenance.
- NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_assertion wasDerivedFrom befree-2016 NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_provenance.
- NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_assertion SIO_000772 16505158 NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_provenance.
- NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_assertion evidence source_evidence_literature NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_provenance.
- NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_assertion description "[Considering all features, CORDX3 is more similar to other X chromosomal cone-rod dystrophies than to CSNB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537770.RAj0Enfw_yalDDIt5vjnQVeKAkUCD-zG4BshE5JGXlzIM130_provenance.