Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_assertion type Assertion NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_head.
- NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_assertion description "[To identify suspected RDS mutations in families in which different people have been identified with either generalised retinal dystrophy or macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_provenance.
- NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_assertion evidence source_evidence_literature NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_provenance.
- NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_assertion SIO_000772 16916875 NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_provenance.
- NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_assertion wasDerivedFrom befree-20150227 NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_provenance.
- NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_assertion wasGeneratedBy ECO_0000203 NP760992.RAa8A_3SwcBNmeoSoDE-WIjrJUu2POfVjk7TMnr4GNnyA130_provenance.