Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_assertion> ?p ?o ?g. }
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- NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_assertion type Assertion NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_head.
- NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_assertion description "[(4) The test is not recommended for children with phenotypes that are not clearly associated with SCN1A mutations such as those characterized by abnormal development or neurologic deficits apparent at birth or structural abnormalities of the brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_provenance.
- NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_assertion evidence source_evidence_literature NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_provenance.
- NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_assertion SIO_000772 23586701 NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_provenance.
- NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_assertion wasDerivedFrom befree-20150227 NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_provenance.
- NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_assertion wasGeneratedBy ECO_0000203 NP682344.RAYYKr_4lc0ECnjnNTjTKT3NVQGbNXCwn3fVtmmmI9cVI130_provenance.