Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_assertion> ?p ?o ?g. }
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- NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_assertion type Assertion NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_head.
- NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_assertion description "[Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_provenance.
- NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_assertion evidence source_evidence_literature NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_provenance.
- NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_assertion SIO_000772 16036915 NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_provenance.
- NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_assertion wasDerivedFrom befree-2016 NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_provenance.
- NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_assertion wasGeneratedBy ECO_0000203 NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_provenance.