Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_provenance.
- NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_assertion description "[While mutations in the NDUFS3 gene thus result in Leigh syndrome, a dissimilar clinical phenotype is observed in mutations in the NDUFV2 and NDUFS2 genes, resulting in encephalomyopathy and cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_provenance.
- NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_assertion evidence source_evidence_literature NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_provenance.
- NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_assertion SIO_000772 14729820 NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_provenance.
- NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_assertion wasDerivedFrom befree-2016 NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_provenance.
- NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_assertion wasGeneratedBy ECO_0000203 NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_provenance.
- befree-2016 importedOn "2016-02-19" NP428484.RATtqqZOUA8iDf8RqXTgOS3FwsebacO3nJ-WQGokOnr8M130_provenance.