Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_assertion type Assertion NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_head.
- NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_assertion description "[Benign familial neonatal convulsions (BFNC, also named benign familial neonatal seizures, BFNS) is a rare autosomal dominant inherited epilepsy syndrome with clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_provenance.
- NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_assertion evidence source_evidence_literature NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_provenance.
- NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_assertion SIO_000772 18249525 NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_provenance.
- NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_assertion wasDerivedFrom befree-20140225 NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_provenance.
- NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_assertion wasGeneratedBy ECO_0000203 NP708773.RAaim9hrCMG8Om1VyYUYgX82XnS196SK4u7gafq8WnRc4130_provenance.