Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_assertion> ?p ?o ?g. }
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- NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_assertion type Assertion NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_head.
- NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_assertion wasGeneratedBy ECO_0000203 NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_provenance.
- NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_assertion wasDerivedFrom befree-20140225 NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_provenance.
- NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_assertion SIO_000772 15761194 NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_provenance.
- NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_assertion evidence source_evidence_literature NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_provenance.
- NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304474.RA0PPsN47SPdY6GXrPEqaVkKUoFc7Sl-nsl3LcqKRmlbU130_provenance.