Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_assertion type Assertion NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_head.
- NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_assertion description "[The 208delG mutation in the FSCN2 gene produces not only autosomal dominant retinitis pigmentosa but also ADMD in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_assertion evidence source_evidence_literature NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_assertion SIO_000772 14609921 NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_assertion wasDerivedFrom befree-20150227 NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_assertion wasGeneratedBy ECO_0000203 NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.