Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_assertion> ?p ?o ?g. }
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- NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_assertion type Assertion NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_head.
- NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_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." NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_provenance.
- NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_assertion evidence source_evidence_literature NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_provenance.
- NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_assertion SIO_000772 14609921 NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_provenance.
- NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_assertion wasDerivedFrom befree-20140225 NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_provenance.
- NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_assertion wasGeneratedBy ECO_0000203 NP664959.RAqX_00Czrx8Bfl0HdAy4Rt30th7fSTL5qoIDBEnQe3pw130_provenance.