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- source_evidence_literature type ECO_0000212 NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP988573.RA1DUlTC8TrMrfZXOohVhKCMc8TGfhhAmqhFDy4JRsjaA130_provenance.