Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_provenance.
- NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_assertion description "[Recent observations suggest that the human episodic ataxia 2 (EA2) and spinocerebellar ataxia types 6 (SCA6), 12 (SCA12), and 14 (SCA14) might be associated with impaired phosphorylation levels of cerebellum calcium channels and receptors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_provenance.
- NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_assertion evidence source_evidence_literature NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_provenance.
- NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_assertion SIO_000772 19488825 NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_provenance.
- NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_assertion wasDerivedFrom befree-2016 NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_provenance.
- NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_assertion wasGeneratedBy ECO_0000203 NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_provenance.
- befree-2016 importedOn "2016-02-19" NP742497.RAnFJRiBeu8_y3sA2m2iSPcc8pWwJMV7Q4qg_bopQhqpE130_provenance.