Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_provenance.
- NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_assertion description "[Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_provenance.
- NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_assertion evidence source_evidence_curated NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_provenance.
- NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_assertion SIO_000772 14702087 NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_provenance.
- NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_assertion wasDerivedFrom uniprot-20150221 NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_provenance.
- NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_assertion wasGeneratedBy ECO_0000218 NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP497.RAaCItralGC9tPDRtno4v2ASaT1_Pa5EeJYxN8wScRj-U130_provenance.