Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_assertion> ?p ?o ?g. }
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- NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_assertion type Assertion NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_head.
- NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_assertion description "[PME can be caused by the juvenile type of Gaucher's disease, which maps to chromosome 1q, by the juvenile type of neuronal ceroid lipofuscinoses (CLN3), which maps to chromosome 16p, and by the `cherry-red-spot-myoclonus` syndrome of Guazzi or sialidosis type I, which has been localized to chromosome 10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_provenance.
- NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_assertion evidence source_evidence_literature NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_provenance.
- NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_assertion SIO_000772 8293722 NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_provenance.
- NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_assertion wasDerivedFrom befree-20140225 NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_provenance.
- NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_assertion wasGeneratedBy ECO_0000203 NP276669.RA2NHq6_LRd2uGekYTYf5ACto852hzWHqhHjj-7chhxWA130_provenance.