Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_assertion> ?p ?o ?g. }
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- NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_assertion type Assertion NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_head.
- NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_assertion description "[Mitochondrial disorder with OPA1 mutation lacking optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_provenance.
- NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_assertion evidence source_evidence_literature NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_provenance.
- NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_assertion SIO_000772 19303950 NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_provenance.
- NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_assertion wasDerivedFrom befree-20140225 NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_provenance.
- NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_assertion wasGeneratedBy ECO_0000203 NP212443.RAVAWrNcoI3WkF1Y1CIP1Bs-1oAXj_lq3nTLk_7gO5RHM130_provenance.