Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_provenance.
- NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_assertion description "[Several mutations in the N terminus of the G-protein-coupled receptor rhodopsin disrupt NXS/T consensus sequences for N-linked glycosylation (located at N2 and N15) and cause sector retinitis pigmentosa in which the inferior retina preferentially degenerates.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_provenance.
- NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_assertion evidence source_evidence_literature NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_provenance.
- NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_assertion SIO_000772 19955366 NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_provenance.
- NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_assertion wasDerivedFrom befree-2016 NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_provenance.
- NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_assertion wasGeneratedBy ECO_0000203 NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_provenance.
- befree-2016 importedOn "2016-02-19" NP778939.RAkTw_sL-ELqBQeGyraoVPCe0wHRIcNv-f4xElOqCH4Sc130_provenance.