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- NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_assertion type Assertion NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_head.
- NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_assertion wasGeneratedBy ECO_0000203 NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_provenance.
- NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_assertion wasDerivedFrom befree-20150227 NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_provenance.
- NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_assertion SIO_000772 8045710 NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_provenance.
- NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_assertion evidence source_evidence_literature NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_provenance.
- NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649194.RAxsKR0lUNb6g_jlBP8DYBnX54tUDx_9cTFCM2RqrJxSE130_provenance.