Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_provenance.
- NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_provenance.
- NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_assertion evidence source_evidence_literature NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_provenance.
- NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_assertion SIO_000772 23941260 NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_provenance.
- NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_assertion wasDerivedFrom befree-2016 NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_provenance.
- NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_assertion wasGeneratedBy ECO_0000203 NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1102140.RAFLpdUjDwQoXHr5BV_u_XN4Y9TZ9KbpsubUZtgophBDg130_provenance.