Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_provenance.
- NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_assertion wasGeneratedBy ECO_0000203 NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_provenance.
- NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_assertion wasDerivedFrom befree-20140225 NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_provenance.
- NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_assertion SIO_000772 19451219 NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_provenance.
- NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_assertion evidence source_evidence_literature NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_provenance.
- NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_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." NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP332902.RA7j5YawHzxKKz-Uw21bTSNwXSQbqj12-WZaoE2p-zr5I130_provenance.