Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_provenance.
- NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_assertion description "[We found increased expression of the mitochondrial fission genes Drp1 and Fis1 (fission 1) and decreased expression of the mitochondrial fusion genes Mfn1 (mitofusin 1), Mfn2 (mitofusin 2), Opa1 (optic atrophy 1) and Tomm40.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_provenance.
- NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_assertion evidence source_evidence_literature NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_provenance.
- NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_assertion SIO_000772 21459773 NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_provenance.
- NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_assertion wasDerivedFrom befree-20150227 NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_provenance.
- NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_assertion wasGeneratedBy ECO_0000203 NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP832552.RAUGX4ZeO2WX22ouf3oVmfj5CE87l59MpBSyVnb5AcIvE130_provenance.