Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_provenance.
- NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_assertion description "[Three patients with AOA1 were identified in an APTX mutation screening on 28 Southern Italian patients with progressive ataxia and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_provenance.
- NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_assertion evidence source_evidence_literature NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_provenance.
- NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_assertion SIO_000772 15596775 NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_provenance.
- NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_assertion wasDerivedFrom befree-20140225 NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_provenance.
- NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_assertion wasGeneratedBy ECO_0000203 NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP298695.RA0JggZHTG9Kj0k8a70HZ9vvVJjhqdPtXqxiC6g0pcJ9o130_provenance.