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- NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_assertion type Assertion NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_head.
- NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_provenance.
- NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_assertion evidence source_evidence_literature NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_provenance.
- NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_assertion SIO_000772 22243967 NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_provenance.
- NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_assertion wasDerivedFrom befree-20140225 NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_provenance.
- NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_assertion wasGeneratedBy ECO_0000203 NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_provenance.