Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_assertion> ?p ?o ?g. }
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- NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_assertion type Assertion NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_head.
- NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_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." NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_assertion evidence source_evidence_literature NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_assertion SIO_000772 22946725 NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_assertion wasDerivedFrom befree-2016 NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_assertion wasGeneratedBy ECO_0000203 NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.