Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_provenance.
- NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_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." NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_provenance.
- NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_assertion evidence source_evidence_literature NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_provenance.
- NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_assertion SIO_000772 17846414 NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_provenance.
- NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_assertion wasDerivedFrom gad-20130706 NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_provenance.
- NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_assertion wasGeneratedBy ECO_0000203 NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_provenance.
- gad-20130706 importedOn "2013-07-06" NP66255.RAdL0CRc_6k6Ng1K8Cdl4tdvRNDvHyyN4Og-U9XyZfbFc130_provenance.