Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_assertion> ?p ?o ?g. }
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- NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_assertion type Assertion NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_head.
- NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_assertion wasGeneratedBy ECO_0000203 NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_provenance.
- NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_assertion wasDerivedFrom befree-20140225 NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_provenance.
- NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_assertion SIO_000772 9359047 NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_provenance.
- NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_assertion evidence source_evidence_literature NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_provenance.
- NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_assertion description "[Homozygosity for EDN3 mutations has been previously shown to cause the Shah-Waardenburg syndrome, a combination of HSCR with features of the Waardenburg syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892882.RAFwj5qZnJI7TBcqiLXMJ24ICPWffEGvlVSqHdLinSlbs130_provenance.