Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_provenance.
- NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_assertion wasGeneratedBy ECO_0000203 NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_provenance.
- NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_assertion wasDerivedFrom befree-20150227 NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_provenance.
- NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_assertion SIO_000772 16200211 NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_provenance.
- NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_assertion evidence source_evidence_literature NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_provenance.
- NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_assertion description "[We found a null mutation in B17.2L in a patient with a progressive encephalopathy and showed that the associated complex I assembly defect could be completely rescued by retroviral expression of B17.2L in patient fibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961085.RA-qaanU02iMaA2wnM34PLR4rB0ncWCAb0NQ8gkMq35x8130_provenance.