Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_assertion> ?p ?o ?g. }
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- NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_assertion type Assertion NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_head.
- NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_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." NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_provenance.
- NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_assertion evidence source_evidence_literature NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_provenance.
- NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_assertion SIO_000772 19847901 NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_provenance.
- NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_assertion wasDerivedFrom befree-2016 NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_provenance.
- NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_assertion wasGeneratedBy ECO_0000203 NP771012.RAFaTdeOHh5ahSFzAkK1AjiGM01bWaKfqBC6h8oBwZCz4130_provenance.