Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_assertion type Assertion NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_head.
- NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_assertion description "[PCDH21 mutations are not a major cause of the retinal diseases investigated herein, and the corresponding human phenotype remains to be determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_provenance.
- NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_assertion evidence source_evidence_literature NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_provenance.
- NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_assertion SIO_000772 16288196 NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_provenance.
- NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_assertion wasDerivedFrom befree-2016 NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_provenance.
- NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_assertion wasGeneratedBy ECO_0000203 NP522764.RAw6xQN43xtlhnmkvo1qsi9QPZDfhZ4zzDEsDhArmUh1w130_provenance.