Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_provenance.
- NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_assertion description "[Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_provenance.
- NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_assertion evidence source_evidence_literature NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_provenance.
- NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_assertion SIO_000772 17486094 NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_provenance.
- NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_assertion wasDerivedFrom befree-20140225 NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_provenance.
- NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_assertion wasGeneratedBy ECO_0000203 NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP621768.RA1Y5dMSLy3EZ8gd-4RIL1gY7xgf8AopdmIyMAad1Dlzo130_provenance.