Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_assertion> ?p ?o ?g. }
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- NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_assertion type Assertion NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_head.
- NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_assertion description "[Unverricht-Lundborg disease (ULD), progressive myoclonic epilepsy type 1 (EPM1, OMIM254800), is an autosomal recessively inherited neurodegenerative disorder characterized by age of onset from 6 to 16 years, stimulus-sensitive myoclonus, and tonic-clonic epileptic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_provenance.
- NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_assertion evidence source_evidence_literature NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_provenance.
- NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_assertion SIO_000772 18325013 NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_provenance.
- NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_assertion wasDerivedFrom befree-2016 NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_provenance.
- NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_assertion wasGeneratedBy ECO_0000203 NP659277.RASaEh7A04nD37pUcR_0EgW3JxL4rPyOyx-oPvft5Ncbw130_provenance.