Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_provenance.
- NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_assertion description "[In two patients heteroplasmic for the base pair (bp) 3243 mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes (MELAS), RRF contained a great excess of mtDNA and transcripts of all species.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_provenance.
- NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_assertion evidence source_evidence_literature NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_provenance.
- NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_assertion SIO_000772 1606473 NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_provenance.
- NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_assertion wasDerivedFrom befree-20140225 NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_provenance.
- NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_assertion wasGeneratedBy ECO_0000203 NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_provenance.
- befree-20140225 importedOn "2014-02-25" NP735082.RAGLctCq44BUnI8WcOzOVjq4KRXxvlm9OJG8BgYqG4-Ck130_provenance.