Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_assertion> ?p ?o ?g. }
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- NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_assertion type Assertion NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_head.
- NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_assertion description "[The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_provenance.
- NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_assertion evidence source_evidence_literature NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_provenance.
- NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_assertion SIO_000772 20811047 NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_provenance.
- NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_assertion wasDerivedFrom befree-20150227 NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_provenance.
- NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_assertion wasGeneratedBy ECO_0000203 NP674851.RAbhrXnCS7IXLXMrdtaNHpptcocY2r0KvpzwudEaT2W00130_provenance.