Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_assertion> ?p ?o ?g. }
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- NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_assertion type Assertion NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_head.
- NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_assertion wasGeneratedBy ECO_0000218 NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_provenance.
- NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_assertion wasDerivedFrom uniprot-20150221 NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_provenance.
- NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_assertion SIO_000772 10079181 NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_provenance.
- NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_assertion evidence source_evidence_curated NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_provenance.
- NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_assertion description "[Recurrent missense (R197C) and nonsense (Y89X) mutations in the XLRS1 gene in families with X-linked retinoschisis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197.RAXSFutqdkfcrHMSUrRPkwYI4rbt2Ajebs8P9nGtBmu4o130_provenance.