Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_provenance.
- NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_assertion description "[We highlight the importance of considering the diagnosis of AOA1 in children with early-onset cerebellar ataxia, once other well-known disorders such as Friedreich's ataxia and ataxia-telangiectasia have been excluded.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_provenance.
- NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_assertion evidence source_evidence_literature NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_provenance.
- NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_assertion SIO_000772 16700949 NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_provenance.
- NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_assertion wasDerivedFrom befree-20150227 NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_provenance.
- NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_assertion wasGeneratedBy ECO_0000203 NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914785.RA7UmDoWFj8uHhZDCZcsUYs4mPuqbJMBHCK399dZOj4uY130_provenance.