Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_assertion type Assertion NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_head.
- NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_assertion description "[A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_provenance.
- NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_assertion evidence source_evidence_literature NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_provenance.
- NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_assertion SIO_000772 25524373 NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_provenance.
- NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_assertion wasDerivedFrom befree-2016 NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_provenance.
- NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_assertion wasGeneratedBy ECO_0000203 NP1249439.RA0EPUcIenh62na1A5EpZ59l8uRs9no4sQ2B9op8j4yX4130_provenance.