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- source_evidence_literature type ECO_0000212 NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_provenance.
- NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_assertion description "[Genetic studies excluded mutations in the DM type 1 (DM1) gene, but revealed a CCTG repeat expansion in the ZNF9 gene, which is associated with DM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_provenance.
- NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_assertion evidence source_evidence_literature NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_provenance.
- NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_assertion SIO_000772 15704146 NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_provenance.
- NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_assertion wasDerivedFrom befree-20140225 NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_provenance.
- NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_assertion wasGeneratedBy ECO_0000203 NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP184919.RAT6q7QaY5iX-GUp4WqRVFipqW7C7fxCdH8LboWKe25Dk130_provenance.