Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_assertion> ?p ?o ?g. }
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- NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_assertion type Assertion NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_head.
- NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_assertion description "[Although we initially focused on the mutation in POLG2, the mutation in OPA1 is more likely to explain the late-onset PEO and multisystem disorder in this patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_provenance.
- NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_assertion evidence source_evidence_literature NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_provenance.
- NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_assertion SIO_000772 18195150 NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_provenance.
- NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_assertion wasDerivedFrom befree-20150227 NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_provenance.
- NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_assertion wasGeneratedBy ECO_0000203 NP602693.RAMnKI7X8QhPJWU5i6bTOIbgryAPB4BI4kr3i3HbONJr0130_provenance.