Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP505281.RAYN_4xLMRfswrtvmwTOBQY98EE6pnjhFQ_cq1p7X4h4U130_provenance.