Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_provenance.
- NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_assertion description "[Further delineation of pontocerebellar hypoplasia type 6 due to mutations in the gene encoding mitochondrial arginyl-tRNA synthetase, RARS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_provenance.
- NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_assertion evidence source_evidence_literature NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_provenance.
- NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_assertion SIO_000772 22086604 NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_provenance.
- NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_assertion wasDerivedFrom befree-2016 NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_provenance.
- NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_assertion wasGeneratedBy ECO_0000203 NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_provenance.
- befree-2016 importedOn "2016-02-19" NP939097.RAvEWUhH5Kw-6VP0CEj_GDXmmyu0c6CvFPOEOl30PyUME130_provenance.