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- source_evidence_literature type ECO_0000212 NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_provenance.
- NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_assertion description "[Myoclonus-dystonia is a movement disorder associated with mutations in the epsilon-sarcoglycan gene (SGCE) in most families and in the DRD2 and DYT1 genes in two single families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_provenance.
- NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_assertion evidence source_evidence_literature NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_provenance.
- NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_assertion SIO_000772 12402271 NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_provenance.
- NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_assertion wasDerivedFrom befree-20150227 NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_provenance.
- NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_assertion wasGeneratedBy ECO_0000203 NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP810920.RAU2pnlQvhyDagUJ5BKbp3ZXIB114zFAB1WJ8esE-HQLs130_provenance.