Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_assertion> ?p ?o ?g. }
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- NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_assertion type Assertion NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_head.
- NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_assertion wasGeneratedBy ECO_0000203 NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_provenance.
- NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_assertion wasDerivedFrom lhgdn-20090331 NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_provenance.
- NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_assertion SIO_000772 12730697 NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_provenance.
- NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_assertion evidence source_evidence_literature NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_provenance.
- NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_assertion description "[two mutations in the gene PCSK9 (encoding proprotein convertase subtilisin/kexin type 9) that cause autosomal dominant hypercholesterolemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134765.RALvyRb2WVJO0XTeanK2pxlOtGClwpqWtXlvK9xg9zfuI130_provenance.