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- source_evidence_literature type ECO_0000212 NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_provenance.
- NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_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." NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_provenance.
- NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_assertion evidence source_evidence_literature NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_provenance.
- NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_assertion SIO_000772 22086604 NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_provenance.
- NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_assertion wasDerivedFrom befree-2016 NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_provenance.
- NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_assertion wasGeneratedBy ECO_0000203 NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_provenance.
- befree-2016 importedOn "2016-02-19" NP939098.RA7Q7mf_1LT89aOvHNfw4iF4HiqsKD55hc4y1Nj2-ZyIo130_provenance.