Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_assertion> ?p ?o ?g. }
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- NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_assertion type Assertion NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_head.
- NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_assertion description "[The authors identified a novel peripherin/RDS gene mutation associated with autosomal dominant retinal degeneration in patients from three different families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_provenance.
- NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_assertion evidence source_evidence_literature NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_provenance.
- NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_assertion SIO_000772 7862413 NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_provenance.
- NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_assertion wasDerivedFrom befree-20150227 NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_provenance.
- NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_assertion wasGeneratedBy ECO_0000203 NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_provenance.