Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_provenance.
- NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_assertion description "[Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_provenance.
- NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_assertion evidence source_evidence_literature NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_provenance.
- NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_assertion SIO_000772 9778262 NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_provenance.
- NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_assertion wasDerivedFrom befree-20150227 NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_provenance.
- NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_assertion wasGeneratedBy ECO_0000203 NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP872999.RApSkJUPkIYY-Icd3r0z8lAj_lPojexOrGU_9M62DRqlM130_provenance.