Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion> ?p ?o ?g. }
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- NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion type Assertion NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_head.
- NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion wasGeneratedBy ECO_0000203 NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion wasDerivedFrom befree-20150227 NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion SIO_000772 9354802 NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion evidence source_evidence_literature NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion description "[Mutations in the hminK gene cause long QT syndrome and suppress IKs function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.