Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_assertion> ?p ?o ?g. }
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- NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_assertion type Assertion NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_head.
- NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_assertion description "[We have analysed the frequency of PRRT2 mutations in families with benign familial infantile convulsions without paroxysmal kinesigenic dyskinesia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_provenance.
- NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_assertion evidence source_evidence_literature NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_provenance.
- NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_assertion SIO_000772 22877996 NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_provenance.
- NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_assertion wasDerivedFrom befree-20140225 NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_provenance.
- NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_assertion wasGeneratedBy ECO_0000203 NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_provenance.