Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_provenance.
- NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_assertion description "[After HARS2, LARS2 is the second gene encoding mitochondrial tRNA synthetase to be found to harbor mutations leading to Perrault syndrome, further supporting�a critical role for mitochondria in the maintenance of ovarian function and hearing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_provenance.
- NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_assertion evidence source_evidence_literature NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_provenance.
- NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_assertion SIO_000772 23541342 NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_provenance.
- NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_assertion wasDerivedFrom befree-20150227 NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_provenance.
- NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_assertion wasGeneratedBy ECO_0000203 NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_provenance.
- befree-20150227 importedOn "2015-02-27" NP873032.RAKZeouTTi23cD2lA2_qo50gRiH4NBdT4lcHgFfAwFbus130_provenance.