Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP265978.RA0XDhjzPCyO4ja95LwcMRKREgW8WHFNZc4CmOpQeY4Yc130_provenance.