Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_assertion type Assertion NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_head.
- NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_assertion wasGeneratedBy ECO_0000203 NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_provenance.
- NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_assertion wasDerivedFrom befree-2016 NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_provenance.
- NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_assertion SIO_000772 21844054 NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_provenance.
- NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_assertion evidence source_evidence_literature NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_provenance.
- NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_assertion description "[It was reported recently that a proportion of patients previously diagnosed with alleged vaccine encephalopathy might possess SCN1A mutations and clinical histories that enabled a diagnosis of Dravet syndrome, but these results have not been replicated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917238.RA_AzGujtXi8dMOVZ6PcZee_jEQUV_8WGHv4vCVzuurR4130_provenance.