Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_assertion> ?p ?o ?g. }
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- NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_assertion type Assertion NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_head.
- NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_assertion description "[Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_provenance.
- NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_assertion evidence source_evidence_curated NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_provenance.
- NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_assertion SIO_000772 11389483 NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_provenance.
- NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_assertion wasDerivedFrom ctd_human-2016 NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_provenance.
- NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_assertion wasGeneratedBy ECO_0000218 NP11313.RAsj8kTc-OBejKd7tR4GxJVaMQgDkcFHcKnGGM57U2XWM130_provenance.