Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_assertion type Assertion NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_head.
- NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_assertion description "[Mutations in PAX6 gene have been shown to be the genetic cause of aniridia, which is a severe panocular eye disease characterised by iris hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_provenance.
- NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_assertion evidence source_evidence_literature NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_provenance.
- NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_assertion SIO_000772 15740668 NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_provenance.
- NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_assertion wasDerivedFrom befree-2016 NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_provenance.
- NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_assertion wasGeneratedBy ECO_0000203 NP483316.RA3GKy-c6jmfEEyBPDm1YVSDxeNuIBZJPL17KoUsWp_Gc130_provenance.