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- NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_assertion type Assertion NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_head.
- NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_assertion wasGeneratedBy ECO_0000203 NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_provenance.
- NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_assertion wasDerivedFrom befree-2016 NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_provenance.
- NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_assertion SIO_000772 24560797 NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_provenance.
- NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_assertion evidence source_evidence_literature NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_provenance.
- NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_assertion description "[Mutations in BEST1 cause five distinct retinal degenerative diseases, including adult vitelliform macular dystrophy (AVMD), autosomal recessive bestrophinopathy (ARB), autosomal dominant vitreoretinochoroidopathy (ADVIRC), and retinitis pigmentosa (RP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1157362.RAF5-r_MU6E2aMYoCLam8PSATWC14-9KtowzwASRO8Z2M130_provenance.