Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_provenance.
- NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_assertion description "[This prompted us to carry out a detailed analysis of the coding region and intron-exon boundaries of POLG1 in Finnish patients with idiopathic sporadic Parkinson disease (PD) and in nonparkinsonian controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_provenance.
- NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_assertion evidence source_evidence_literature NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_provenance.
- NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_assertion SIO_000772 17846414 NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_provenance.
- NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_assertion wasDerivedFrom befree-20150227 NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_provenance.
- NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_assertion wasGeneratedBy ECO_0000203 NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP633490.RAMMAs_3uvNcYkh9VfqW79QTBmoYgAKJ1knZ1TmJHv38M130_provenance.