Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_assertion> ?p ?o ?g. }
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- NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_assertion type Assertion NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_head.
- NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_assertion description "[Clinically, POLG mutations can present from early neonatal life to late middle age, with a spectrum of phenotypes that includes common neurological disorders such as migraine, epilepsy and Parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_provenance.
- NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_assertion evidence source_evidence_literature NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_provenance.
- NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_assertion SIO_000772 16987890 NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_provenance.
- NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_assertion wasDerivedFrom befree-20140225 NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_provenance.
- NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_assertion wasGeneratedBy ECO_0000203 NP812285.RAhDvq4eDwql4TzhFrHnvE4Kxo2UhUmERpqqH-KNHH6-Q130_provenance.