Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_assertion> ?p ?o ?g. }
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- NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_assertion type Assertion NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_head.
- NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_assertion description "[By genotyping several putative disease loci using microsatellite markers we were able to describe a new NDUFS7 mutation in a consanguineous family with Leigh syndrome and isolated complex I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_provenance.
- NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_assertion evidence source_evidence_literature NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_provenance.
- NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_assertion SIO_000772 17604671 NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_provenance.
- NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_assertion wasDerivedFrom befree-20150227 NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_provenance.
- NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_assertion wasGeneratedBy ECO_0000203 NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_provenance.