Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_assertion type Assertion NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_head.
- NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_assertion description "[A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_provenance.
- NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_assertion evidence source_evidence_literature NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_provenance.
- NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_assertion SIO_000772 8485575 NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_provenance.
- NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_assertion wasDerivedFrom befree-2016 NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_provenance.
- NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_assertion wasGeneratedBy ECO_0000203 NP1343022.RAbeYz1XThWAJlzSJhAvlZnK69jaKU2D6yLe8n_zltMNg130_provenance.