Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_provenance.
- NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_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." NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_provenance.
- NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_assertion evidence source_evidence_literature NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_provenance.
- NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_assertion SIO_000772 16987890 NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_provenance.
- NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_assertion wasDerivedFrom befree-20140225 NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_provenance.
- NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_assertion wasGeneratedBy ECO_0000203 NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP378784.RA72Oj5ur8galajxiYmiJWCoj-_qXWtWtFitLFriVhLlA130_provenance.