Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_assertion> ?p ?o ?g. }
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- NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_assertion type Assertion NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_head.
- NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_assertion description "[Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_provenance.
- NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_assertion evidence source_evidence_literature NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_provenance.
- NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_assertion SIO_000772 16648378 NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_provenance.
- NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_assertion wasDerivedFrom befree-20140225 NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_provenance.
- NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_assertion wasGeneratedBy ECO_0000203 NP502599.RAGOvS6FAA96uBOqycJe2cwZ3mcVR2D4B-lwOw96taLoY130_provenance.