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- NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_assertion type Assertion NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_head.
- NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_assertion description "[Specifically, we detected pathogenic DNA variants (?50% novel mutations) in the genes RP1, USH2A, CNGB3, NMNAT1, CHM, and ABCA4, responsible for retinitis pigmentosa, Usher syndrome, achromatopsia, Leber congenital amaurosis, choroideremia, or recessive Stargardt/cone-rod dystrophy cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_provenance.
- NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_assertion evidence source_evidence_literature NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_provenance.
- NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_assertion SIO_000772 23940504 NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_provenance.
- NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_assertion wasDerivedFrom befree-20140225 NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_provenance.
- NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_assertion wasGeneratedBy ECO_0000203 NP396780.RAAy_Pt-8iphLyYwyDnlwBLcp19Wgk_uEI7MDvlFo9psw130_provenance.