Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_provenance.
- NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_assertion description "[We conclude that, independent of precise syndromic delineation, myoclonic-astatic seizures are not predictive of SCN1A mutations in sporadic myoclonic epilepsies of infancy and early childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_provenance.
- NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_assertion evidence source_evidence_literature NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_provenance.
- NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_assertion SIO_000772 15944908 NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_provenance.
- NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_assertion wasDerivedFrom befree-20150227 NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_provenance.
- NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_assertion wasGeneratedBy ECO_0000203 NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682404.RAjSSOyqSt7hxVvN2erNjlBsKeFuqVpIr1Ikekxvqk5CM130_provenance.