Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP669014.RAXpf6b3bd3Jds8vn_FeZnl1T4hPsZYYNnIaAHx4nzpWM130_provenance.