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- NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_assertion type Assertion NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_head.
- NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_assertion description "[We hypothesized that mutations in SCARB2 might account for unsolved cases of progressive myoclonus epilepsy (PME) without renal impairment, especially those resembling Unverricht-Lundborg disease (ULD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_provenance.
- NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_assertion evidence source_evidence_literature NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_provenance.
- NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_assertion SIO_000772 19847901 NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_provenance.
- NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_assertion wasDerivedFrom befree-20140225 NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_provenance.
- NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_assertion wasGeneratedBy ECO_0000203 NP716315.RAv5xdIkbl7gHLDORcmpVP89JZu4md2S-uO23I1AWWVU8130_provenance.