Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_provenance.
- NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_assertion description "[Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_provenance.
- NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_assertion evidence source_evidence_curated NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_provenance.
- NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_assertion SIO_000772 23857908 NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_provenance.
- NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_assertion wasDerivedFrom uniprot-2016 NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_provenance.
- NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_assertion wasGeneratedBy ECO_0000218 NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7588.RAOJ69Ud-tgwivvYxBxWma2zow6OwpfPJiDpy_4H-LNhw130_provenance.