Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_assertion> ?p ?o ?g. }
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- NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_assertion type Assertion NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_head.
- NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_assertion description "[Recently, mutations in LCA5, encoding the ciliary protein lebercilin, were reported to be a rare cause of leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_provenance.
- NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_assertion evidence source_evidence_literature NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_provenance.
- NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_assertion SIO_000772 18000884 NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_provenance.
- NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_assertion wasDerivedFrom befree-20150227 NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_provenance.
- NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_assertion wasGeneratedBy ECO_0000203 NP977701.RASEbc7bFwXmdgc4cSQoaMrugQk20c-Wq5xvLmspCgPwU130_provenance.