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- NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_assertion type Assertion NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_head.
- NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_assertion description "[Long-term follow-up of the human phenotype in three siblings with cone dystrophy associated with a homozygous p.G461R mutation of KCNV2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_assertion evidence source_evidence_literature NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_assertion SIO_000772 21911584 NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_assertion wasDerivedFrom befree-20140225 NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_assertion wasGeneratedBy ECO_0000203 NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.