Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_assertion> ?p ?o ?g. }
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- NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_assertion type Assertion NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_head.
- NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_assertion description "[The purpose of the present study was to determine the utility and limitations of haplotype-based genetic mapping in estimating the location of the NYX gene, which has recently been identified as the causative gene for a rare inherited retinal disorder known as the complete type of X-linked congenital stationary night blindness (CSNB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_provenance.
- NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_assertion evidence source_evidence_literature NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_provenance.
- NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_assertion SIO_000772 11408949 NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_provenance.
- NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_assertion wasDerivedFrom befree-20150227 NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_provenance.
- NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_assertion wasGeneratedBy ECO_0000203 NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_provenance.