Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_assertion> ?p ?o ?g. }
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- NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_assertion type Assertion NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_head.
- NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_assertion wasGeneratedBy ECO_0000218 NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_provenance.
- NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_assertion wasDerivedFrom uniprot-20130724 NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_provenance.
- NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_assertion SIO_000772 15051636 NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_provenance.
- NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_assertion evidence source_evidence_curated NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_provenance.
- NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_assertion description "[Compound mutations: a common cause of severe long-QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3416.RATAX0F3nv3hxKK1reTBC6HBF_rzOChsQUTGW3sDbXIHE130_provenance.