Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_provenance.
- NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_assertion description "[Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_provenance.
- NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_assertion evidence source_evidence_literature NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_provenance.
- NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_assertion SIO_000772 23541342 NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_provenance.
- NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_assertion wasDerivedFrom befree-20140225 NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_provenance.
- NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_assertion wasGeneratedBy ECO_0000203 NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP569399.RA_PD9mcmyY2bw2W1wEhh7QZOl7AKfkvID_SjJvWAFoLo130_provenance.