Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_assertion> ?p ?o ?g. }
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- NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_assertion type Assertion NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_head.
- NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_provenance.
- NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_assertion evidence source_evidence_literature NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_provenance.
- NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_assertion SIO_000772 22178368 NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_provenance.
- NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_assertion wasDerivedFrom befree-20140225 NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_provenance.
- NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_assertion wasGeneratedBy ECO_0000203 NP409102.RAnhIkw9iyZ7rSYk8AD7RD2j5zAe3LQh4ZMlE6f9VRja0130_provenance.