Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_provenance.
- NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_assertion description "[POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_provenance.
- NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_assertion evidence source_evidence_literature NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_provenance.
- NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_assertion SIO_000772 16682683 NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_provenance.
- NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_assertion wasDerivedFrom befree-20150227 NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_provenance.
- NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_assertion wasGeneratedBy ECO_0000203 NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_provenance.