Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_assertion> ?p ?o ?g. }
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- NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_assertion type Assertion NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_head.
- NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_assertion wasGeneratedBy ECO_0000203 NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_provenance.
- NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_assertion wasDerivedFrom lhgdn-20090331 NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_provenance.
- NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_assertion SIO_000772 15235026 NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_provenance.
- NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_assertion evidence source_evidence_literature NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_provenance.
- NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_assertion description "[A patient with typical clinical and neuroradiological features of Leigh syndrome and cytochrome oxidase deficiency was found to have a mutation in the COX15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_provenance.