Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
- NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion wasGeneratedBy ECO_0000218 NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
- NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion wasDerivedFrom uniprot-20130724 NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
- NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion SIO_000772 16384941 NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
- NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion evidence source_evidence_curated NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
- NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.