Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_provenance.
- NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_assertion description "[The expansion of a CAG repeat upstream of the PP2APR55beta gene has been recently reported as a novel cause of a dominantly inherited ataxia (SCA12) in a kindred with limb tremor as an early feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_provenance.
- NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_assertion evidence source_evidence_literature NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_provenance.
- NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_assertion SIO_000772 11708992 NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_provenance.
- NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_assertion wasDerivedFrom befree-2016 NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_provenance.
- NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_assertion wasGeneratedBy ECO_0000203 NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_provenance.
- befree-2016 importedOn "2016-02-19" NP336440.RArVydtAxqPVMMJ7TRIDUQPgCeiMzQ3GRd855MLyMAIn0130_provenance.