Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP871490.RA39ONh7acMzXnRdV6epC9tUKtdBai9tsxavZmMT4Q3io130_provenance.