Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_assertion> ?p ?o ?g. }
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- NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_assertion type Assertion NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_head.
- NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_assertion description "[novel nonsense mutations in 2 African American siblings with autosomal recessive Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_provenance.
- NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_assertion evidence source_evidence_literature NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_provenance.
- NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_assertion SIO_000772 18436078 NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_provenance.
- NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_assertion wasDerivedFrom lhgdn-20090331 NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_provenance.
- NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_assertion wasGeneratedBy ECO_0000203 NP237116.RAFBdY4nAB7WCJjsWagDc3vWWjbnkfE8_BaxfXM2zHVeA130_provenance.