Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_assertion type Assertion NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_head.
- NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_assertion wasGeneratedBy ECO_0000218 NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_provenance.
- NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_assertion wasDerivedFrom uniprot-20130724 NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_provenance.
- NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_assertion SIO_000772 20560207 NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_provenance.
- NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_assertion evidence source_evidence_curated NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_provenance.
- NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_assertion description "[Identification of a Kir3.4 mutation in congenital long QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3456.RAUZ7aszcf2jdCdUAxNjUsJ4DecNS9IP_OGRACX7QacQM130_provenance.