Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_provenance.
- NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_assertion description "[CHMP4B, a novel gene for autosomal dominant cataracts linked to chromosome 20q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_provenance.
- NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_assertion evidence source_evidence_curated NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_provenance.
- NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_assertion SIO_000772 17701905 NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_provenance.
- NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_assertion wasDerivedFrom uniprot-2016 NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_provenance.
- NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_assertion wasGeneratedBy ECO_0000218 NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP5091.RAsRGpWxQRbalR3ZbjblSS1sD3opLJZKKHKD3Zw6DVJ9I130_provenance.