Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_provenance.
- NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_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." NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_provenance.
- NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_assertion evidence source_evidence_literature NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_provenance.
- NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_assertion SIO_000772 17486094 NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_provenance.
- NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_assertion wasDerivedFrom befree-20140225 NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_provenance.
- NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_assertion wasGeneratedBy ECO_0000203 NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP365677.RApc4Zg4ieT7cJdF6-yjsGO6fHhyqIPT-33mzsoX2591s130_provenance.