Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_provenance.
- NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_assertion description "[We investigated 30 patients with familial essential tremor (ET) for spinocerebellar ataxia type 12 (SCA-12) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_provenance.
- NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_assertion evidence source_evidence_literature NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_provenance.
- NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_assertion SIO_000772 12210890 NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_provenance.
- NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_assertion wasDerivedFrom befree-20150227 NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_provenance.
- NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_assertion wasGeneratedBy ECO_0000203 NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP638813.RAb8jmQ2VEZk7NzIwsVosU7s8vgTa2pYMo2aRe-amVUtg130_provenance.