Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_provenance.