Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_provenance.
- NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_assertion description "[We conclude that mutations in the EFHC1 gene may underlie different types of epilepsy syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_provenance.
- NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_assertion evidence source_evidence_literature NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_provenance.
- NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_assertion SIO_000772 17159113 NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_provenance.
- NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_assertion wasDerivedFrom befree-2016 NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_provenance.
- NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_assertion wasGeneratedBy ECO_0000203 NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_provenance.
- befree-2016 importedOn "2016-02-19" NP583518.RALY5qENsDeFusu5blLYXFfHwtgL5ypPTRwT5utV8UsAI130_provenance.