Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion> ?p ?o ?g. }
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- NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion type Assertion NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_head.
- NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion description "[To investigate whether Leber's hereditary optic neuropathy (LHON) could be caused by mutations in OPA1 we also screened a panel of 28 LHON patients who tested negatively for the three major LHON mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion evidence source_evidence_literature NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion SIO_000772 11440989 NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion wasDerivedFrom befree-20140225 NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.
- NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_assertion wasGeneratedBy ECO_0000203 NP219307.RAuplxzHpNMtrfy5TzGObU-qS3IkNKjD9Cfg57ptMoTok130_provenance.