Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_assertion type Assertion NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_head.
- NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_assertion description "[A high frequency of epilepsy (43%) was observed in our patients with GLUD1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_provenance.
- NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_assertion evidence source_evidence_literature NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_provenance.
- NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_assertion SIO_000772 19690084 NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_provenance.
- NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_assertion wasDerivedFrom befree-20150227 NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_provenance.
- NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_assertion wasGeneratedBy ECO_0000203 NP429022.RA284v0USLP5WoXHyGfwG1lr5HhWkuh7gXpRv3hQyQJww130_provenance.