Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion type Assertion NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_head.
- NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion description "[The authors identified a novel peripherin/RDS gene mutation associated with autosomal dominant retinal degeneration in patients from three different families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion evidence source_evidence_literature NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion SIO_000772 7862413 NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion wasDerivedFrom befree-20140225 NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion wasGeneratedBy ECO_0000203 NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.