Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_assertion> ?p ?o ?g. }
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- NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_assertion type Assertion NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_head.
- NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_assertion wasGeneratedBy ECO_0000203 NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_provenance.
- NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_assertion wasDerivedFrom befree-20150227 NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_provenance.
- NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_assertion SIO_000772 23942138 NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_provenance.
- NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_assertion evidence source_evidence_literature NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_provenance.
- NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_assertion description "[SLCO1B1 genetic variant associated with statin-induced myopathy: a proof-of-concept study using the clinical practice research datalink.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366199.RA3T10XRQu1fvJIMVDi7O_hYbu1VOZHQs3TKWv4puG7-I130_provenance.