Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_assertion> ?p ?o ?g. }
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- NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_assertion type Assertion NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_head.
- NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_provenance.
- NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_assertion evidence source_evidence_literature NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_provenance.
- NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_assertion SIO_000772 17314340 NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_provenance.
- NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_assertion wasDerivedFrom befree-20150227 NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_provenance.
- NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_assertion wasGeneratedBy ECO_0000203 NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_provenance.