Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_provenance.
- NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_assertion description "[We selected 20 families with epilepsy and migraine and performed mutation analysis of ATP1A2 in the probands by direct sequencing of all exons and splice-site junctions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_provenance.
- NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_assertion evidence source_evidence_literature NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_provenance.
- NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_assertion SIO_000772 18028407 NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_provenance.
- NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_assertion wasDerivedFrom befree-2016 NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_provenance.
- NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_assertion wasGeneratedBy ECO_0000203 NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP641458.RATpQ03yTY8SbuYeltPUhAqPtjFGbgel43ywVzHUWdp4Y130_provenance.