Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_assertion> ?p ?o ?g. }
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- NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_assertion type Assertion NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_head.
- NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_assertion description "[The 208delG mutation in the FSCN2 gene produces not only autosomal dominant retinitis pigmentosa but also ADMD (autosomal dominant macular degeneration)]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_provenance.
- NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_assertion evidence source_evidence_literature NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_provenance.
- NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_assertion SIO_000772 14609921 NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_provenance.
- NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_assertion wasDerivedFrom lhgdn-20090331 NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_provenance.
- NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_assertion wasGeneratedBy ECO_0000203 NP201363.RAEmgVCNKHJa4GYsI_Aylz4W7_H1n_4JaNi8O-9jhVhGY130_provenance.