Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_provenance.
- NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_assertion description "[In myotonic dystrophy type 1 (DM1), alternative splicing of ryanodine receptor 1 (RyR1) and sarcoplasmic/endoplasmic reticulum Ca2+ ATPase (SERCA) genes has been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_provenance.
- NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_assertion evidence source_evidence_literature NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_provenance.
- NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_assertion SIO_000772 17661063 NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_provenance.
- NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_assertion wasDerivedFrom befree-20140225 NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_provenance.
- NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_assertion wasGeneratedBy ECO_0000203 NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP506929.RAgcQISx-XR9j3lUdmto9GF7qz_8N6K6u8pTf2TxFIMVg130_provenance.