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- source_evidence_literature type ECO_0000212 NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_provenance.
- NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_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." NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_provenance.
- NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_assertion evidence source_evidence_literature NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_provenance.
- NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_assertion SIO_000772 19955366 NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_provenance.
- NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_assertion wasDerivedFrom befree-20140225 NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_provenance.
- NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_assertion wasGeneratedBy ECO_0000203 NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP739997.RAWq9TnPwLItSeK-NnGAv2C7sG-xN1pFoZCmEzZznW_Hs130_provenance.