Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_provenance.
- NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_assertion description "[ABCA 4 mutations are responsible for a large variety of retinal degenerations including all cases of Stargardt macular dystrophy and fundus flavimaculatus, some forms of cone-rod degeneration, and retinitis pigmentosa, and likely increase the risk of developing age-related macular degeneration (AMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_provenance.
- NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_assertion evidence source_evidence_literature NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_provenance.
- NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_assertion SIO_000772 12789571 NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_provenance.
- NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_assertion wasDerivedFrom befree-20140225 NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_provenance.
- NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_assertion wasGeneratedBy ECO_0000203 NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_provenance.
- befree-20140225 importedOn "2014-02-25" NP442529.RANqMM_xCOx5bhS9rA8KlLWHnD3VWdK_yODAJMzTOdH04130_provenance.