Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_provenance.
- NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_assertion wasGeneratedBy ECO_0000203 NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_provenance.
- NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_assertion wasDerivedFrom befree-20150227 NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_provenance.
- NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_assertion SIO_000772 24225340 NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_provenance.
- NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_assertion evidence source_evidence_literature NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_provenance.
- NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_assertion description "[SCN1A mutated patients (n = 58) seemed to exhibit worse psychomotor course than non-mutated ones (n = 9) (severe SQPS in 26% vs 0%), although their epilepsy tended to be less severe (tonic seizures in 12% vs 44% [p = 0.04], first status epilepticus before 6 m in 26% vs 67% [p = .02], mean number of SE 2.5 vs 4.5 [p = .09]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682445.RAuOb4pbVJAXDxKi_4KhSvZe1pve8TnjdQJNGrrm8q3dc130_provenance.