Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_provenance.
- NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_assertion wasGeneratedBy ECO_0000203 NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_provenance.
- NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_assertion wasDerivedFrom befree-20150227 NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_provenance.
- NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_assertion SIO_000772 19451219 NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_provenance.
- NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_assertion evidence source_evidence_literature NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_provenance.
- NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_assertion description "[Additionally, our Cisd2 knockout mouse work provides strong evidence supporting an earlier clinical hypothesis that WFS is in part a mitochondria-mediated disorder; specifically, we propose that mutation of CISD2 causes the mitochondria-mediated disorder WFS2 in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776989.RApd0pxrNv8b5LWsxVA5zHQGj1NrE2jaA_PJSDW30nbpo130_provenance.