Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_assertion> ?p ?o ?g. }
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- NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_assertion type Assertion NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_head.
- NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_assertion description "[The aim of our study was to determine whether mutations of the TCF8 gene, recently implicated in posterior polymorphous dystrophy, may also play a role in the development of the more common Fuchs endothelial corneal dystrophy (FECD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_provenance.
- NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_assertion evidence source_evidence_literature NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_provenance.
- NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_assertion SIO_000772 18172091 NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_provenance.
- NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_assertion wasDerivedFrom befree-20140225 NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_provenance.
- NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_assertion wasGeneratedBy ECO_0000203 NP615321.RAEe-kTXdVSPm4QtHG8YEFo-xD3rWLMAqfI47QUuGUHWE130_provenance.