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- source_evidence_literature type ECO_0000212 NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP649184.RAX4KekcB_98WHtr8kHr-ZpWKURBSU_RF7J0io9pMnyic130_provenance.