Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_assertion> ?p ?o ?g. }
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- NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_assertion type Assertion NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_head.
- NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_assertion description "[in a kindred with a syndrome including hypertension, hypercholesterolemia & hypomagnesemia, analysis of maternal lineage mitochondrial genome identified a mutation substituting cytidine for uridine immediately 5'to the mitochondrial TRNA (Ile) anticodon ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_provenance.
- NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_assertion evidence source_evidence_literature NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_provenance.
- NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_assertion SIO_000772 15498972 NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_provenance.
- NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_assertion wasDerivedFrom lhgdn-20090331 NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_provenance.
- NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_assertion wasGeneratedBy ECO_0000203 NP135499.RAC3GUxmM_x9feYRUtibX59xT-Hf5sYMuZTvZ35WcKRyw130_provenance.