Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion> ?p ?o ?g. }
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- NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion type Assertion NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_head.
- NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion description "[They include well-recognized syndromes such as tuberous sclerosis complex, epilepsy associated with Rett syndrome, some of the progressive myoclonic epilepsies, and novel disorders such as epilepsy associated with mutations in the PCDH 19 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion evidence source_evidence_literature NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion SIO_000772 22946725 NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion wasDerivedFrom befree-20140225 NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.
- NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_assertion wasGeneratedBy ECO_0000203 NP615921.RAsxYswQDVjspa4G2tD0ljj0WksZscE1_fvwEmvFZ0lQY130_provenance.