Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_provenance.
- NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_assertion description "[Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_provenance.
- NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_assertion evidence source_evidence_curated NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_provenance.
- NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_assertion SIO_000772 20473310 NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_provenance.
- NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_assertion wasDerivedFrom ctd_human-2016 NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_provenance.
- NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_assertion wasGeneratedBy ECO_0000218 NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP26156.RAA6CohV6fmGfVFqOaTBtQx7Qq1WG4OLHQ7ku2lF5WPWI130_provenance.