Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_assertion> ?p ?o ?g. }
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- NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_assertion type Assertion NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_head.
- NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_assertion description "[Many novel ATP1A2 mutations were identified in patients with familial and sporadic hemiplegic migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_provenance.
- NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_assertion evidence source_evidence_literature NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_provenance.
- NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_assertion SIO_000772 18451712 NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_provenance.
- NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_assertion wasDerivedFrom befree-2016 NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_provenance.
- NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_assertion wasGeneratedBy ECO_0000203 NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_provenance.