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- NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_assertion type Assertion NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_head.
- NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_assertion description "[These results indicate that the KCNJ13 R162W mutation can cause SVD and further show that vitreoretinal degeneration can arise through mutations in genes whose products are not structural components of the vitreous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_provenance.
- NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_assertion evidence source_evidence_literature NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_provenance.
- NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_assertion SIO_000772 18179896 NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_provenance.
- NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_assertion wasDerivedFrom befree-20150227 NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_provenance.
- NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_assertion wasGeneratedBy ECO_0000203 NP522835.RAWA3jn00-wzbFONPpyFxAWSAmRAUHafnKh4vRvNLjNPE130_provenance.