Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_assertion> ?p ?o ?g. }
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- NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_assertion type Assertion NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_head.
- NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_assertion description "[An A8296G mutation in the MT-TK gene of a patient with epilepsy - a disease-causing mutation or rare polymorphism?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_provenance.
- NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_assertion evidence source_evidence_literature NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_provenance.
- NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_assertion SIO_000772 18651333 NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_provenance.
- NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_assertion wasDerivedFrom befree-20140225 NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_provenance.
- NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_assertion wasGeneratedBy ECO_0000203 NP755005.RAt0TvUVid7e-sb5tldSdKvEfd2YbSLzvIIMahizYJ9yw130_provenance.