Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_assertion> ?p ?o ?g. }
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- NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_assertion type Assertion NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_head.
- NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_assertion wasGeneratedBy ECO_0000203 NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_provenance.
- NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_assertion wasDerivedFrom befree-2016 NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_provenance.
- NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_assertion SIO_000772 19220312 NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_provenance.
- NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_assertion evidence source_evidence_literature NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_provenance.
- NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_assertion description "[The results extend the clinical spectrum associated with SCN1A mutations and further strengthen the molecular evidence that FHM and epilepsy share, at least in part, similar molecular pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720776.RA0DDHspbQlKoWzy1che--NCLAUAU73TJRYPYKRwf4tCo130_provenance.