Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_assertion> ?p ?o ?g. }
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- NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_assertion type Assertion NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_head.
- NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_assertion description "[SPG7 is a newly identified gene involved in an autosomal recessive form of hereditary spastic paraplegia (HSP), a genetically heterogeneous group of neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_provenance.
- NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_assertion evidence source_evidence_literature NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_provenance.
- NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_assertion SIO_000772 10480368 NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_provenance.
- NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_assertion wasDerivedFrom befree-20140225 NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_provenance.
- NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_assertion wasGeneratedBy ECO_0000203 NP565409.RA0WpY5y8noZaNnCGWR5WAQpoN3dnTSN3P0e-oM1OoLjI130_provenance.