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- NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_assertion type Assertion NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_head.
- NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_assertion wasGeneratedBy ECO_0000203 NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_provenance.
- NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_assertion wasDerivedFrom befree-20140225 NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_provenance.
- NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_assertion SIO_000772 8045710 NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_provenance.
- NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_assertion evidence source_evidence_literature NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_provenance.
- NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_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." NP552068.RAgF8Yy8_osow4Tr5BZ1Euq3Lhtr_ivSrM6tJla5U7ID8130_provenance.