Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_assertion> ?p ?o ?g. }
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- NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_assertion type Assertion NP877685.RAgqsbW19eCa1mVOTMA-Ctc8fX4TprGJXzcsJI5SX0HLs130_head.
- 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.