Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_provenance.
- NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_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." NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_provenance.
- NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_assertion evidence source_evidence_literature NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_provenance.
- NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_assertion SIO_000772 12210890 NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_provenance.
- NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_assertion wasDerivedFrom befree-20140225 NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_provenance.
- NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_assertion wasGeneratedBy ECO_0000203 NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP548761.RAisjnUetK9RX0MHHgcVrPXgzUpeWYNQQ6V1sWT2xAW5c130_provenance.