Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_assertion type Assertion NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_head.
- NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_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." NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_provenance.
- NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_assertion evidence source_evidence_curated NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_provenance.
- NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_assertion SIO_000772 16384941 NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_provenance.
- NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_assertion wasDerivedFrom ctd_human-20150221 NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_provenance.
- NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_assertion wasGeneratedBy ECO_0000218 NP19457.RAkvkirJlbBMskIUm8Rw_EP0HnzHJkoq4UBnYznhC9T2U130_provenance.