Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_provenance.
- befree-2016 importedOn "2016-02-19" NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_provenance.
- NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_assertion wasGeneratedBy ECO_0000203 NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_provenance.
- NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_assertion wasDerivedFrom befree-2016 NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_provenance.
- NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_assertion SIO_000772 21035104 NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_provenance.
- NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_assertion evidence source_evidence_literature NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_provenance.
- NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_assertion description "[We have identified missense mutations in prodynorphin (PDYN) that cause SCA23 in four Dutch families displaying progressive gait and limb ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849098.RA1hBUUYSLsWsRJ7_Yu2jeir6V_QDTr5aLe2GKDJwzhhA130_provenance.