Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_assertion> ?p ?o ?g. }
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- NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_assertion type Assertion NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_head.
- NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_assertion description "[Mutations in ATP13A2 (PARK9), encoding a lysosomal P-type ATPase, are associated with both Kufor-Rakeb syndrome (KRS) and neuronal ceroid lipofuscinosis (NCL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_provenance.
- NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_assertion evidence source_evidence_literature NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_provenance.
- NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_assertion SIO_000772 23393156 NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_provenance.
- NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_assertion wasDerivedFrom befree-20150227 NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_provenance.
- NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_assertion wasGeneratedBy ECO_0000203 NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_provenance.