Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_assertion> ?p ?o ?g. }
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- NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_assertion type Assertion NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_head.
- NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_assertion wasGeneratedBy ECO_0000203 NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_provenance.
- NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_assertion wasDerivedFrom befree-20150227 NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_provenance.
- NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_assertion SIO_000772 16272056 NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_provenance.
- NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_assertion evidence source_evidence_literature NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_provenance.
- NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_assertion description "[Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) have recently been discovered to cause a form of autosomal dominant retinitis pigmentosa (adRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509542.RACVmBe9Wdkzis_9372nKetyPuXnXpNvAlRYrM1e0Uorw130_provenance.