Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_assertion> ?p ?o ?g. }
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- NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_assertion type Assertion NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_head.
- NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_assertion wasGeneratedBy ECO_0000218 NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_provenance.
- NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_assertion wasDerivedFrom uniprot-2016 NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_provenance.
- NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_assertion SIO_000772 20560207 NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_provenance.
- NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_assertion evidence source_evidence_curated NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_provenance.
- NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_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." NP6259.RAt8pOY5TTeBLH5ceLedgbhHq_NZmC19jYeJhogId5oug130_provenance.