Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_provenance.
- NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_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." NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_provenance.
- NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_assertion evidence source_evidence_literature NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_provenance.
- NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_assertion SIO_000772 19955366 NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_provenance.
- NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_assertion wasDerivedFrom befree-20140225 NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_provenance.
- NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_assertion wasGeneratedBy ECO_0000203 NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP885270.RATD57U3MfDZbe2ARzA3TE-_TcvW35PGvgABtc-DpPv9M130_provenance.