Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion> ?p ?o ?g. }
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- NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion type Assertion NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_head.
- 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.
- NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion evidence source_evidence_curated NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
- NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion SIO_000772 16384941 NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
- NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion wasDerivedFrom uniprot-20130724 NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.
- NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_assertion wasGeneratedBy ECO_0000218 NP3252.RAQpHIBbQ51V530395GPAEhTr87dC39N78m08mgHvxYXw130_provenance.