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- source_evidence_literature type ECO_0000212 NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_provenance.
- NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_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." NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_provenance.
- NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_assertion evidence source_evidence_literature NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_provenance.
- NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_assertion SIO_000772 19955366 NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_provenance.
- NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_assertion wasDerivedFrom befree-20150227 NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_provenance.
- NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_assertion wasGeneratedBy ECO_0000203 NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP928122.RAhXU7WwCPFup5SOZ2_iGpnWM6JwraMDm9CO_Jyf9AE9A130_provenance.