Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_assertion> ?p ?o ?g. }
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- NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_assertion type Assertion NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_head.
- NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_assertion wasGeneratedBy ECO_0000203 NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_provenance.
- NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_assertion wasDerivedFrom befree-20150227 NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_provenance.
- NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_assertion SIO_000772 16384941 NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_provenance.
- NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_assertion evidence source_evidence_literature NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_provenance.
- NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_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." NP509549.RAk8QIaxPEOii0oWNkntDuFav-uwmxfdNgXnx8WT-YgaE130_provenance.