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- source_evidence_literature type ECO_0000212 NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_provenance.
- befree-2016 importedOn "2016-02-19" NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_provenance.
- NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_assertion wasGeneratedBy ECO_0000203 NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_provenance.
- NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_assertion wasDerivedFrom befree-2016 NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_provenance.
- NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_assertion SIO_000772 21694734 NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_provenance.
- NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_assertion evidence source_evidence_literature NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_provenance.
- NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_assertion description "[Finally, we provide evidence that ISS in deletion 1p36 may be associated with deletion of KLHL17 and expand the epilepsy phenotype in that syndrome to include early infantile epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP904007.RA9L5UJCkurttulW2OnAOx315NZl35C6CjOatxPHHJcZw130_provenance.