Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_provenance.
- NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_assertion description "[Mutations in the receptor expression enhancing protein 1 (REEP1) gene have recently been reported to be associated with an autosomal dominant HSP phenotype (SPG31).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_provenance.
- NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_assertion evidence source_evidence_literature NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_provenance.
- NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_assertion SIO_000772 19034539 NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_provenance.
- NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_assertion wasDerivedFrom befree-2016 NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_provenance.
- NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_assertion wasGeneratedBy ECO_0000203 NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_provenance.
- befree-2016 importedOn "2016-02-19" NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_provenance.