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- source_evidence_literature type ECO_0000212 NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_provenance.
- NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_assertion description "[Mutations in the DYT1 gene can cause focal dystonia, and an association with a polymorphism in the D5 receptor gene (DRD5) has been reported but not confirmed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_provenance.
- NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_assertion evidence source_evidence_literature NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_provenance.
- NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_assertion SIO_000772 14581671 NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_provenance.
- NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_assertion wasDerivedFrom befree-2016 NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_provenance.
- NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_assertion wasGeneratedBy ECO_0000203 NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_provenance.
- befree-2016 importedOn "2016-02-19" NP418447.RAIk6bW2N-J9PHVhZrZs9YGyghOlvavC-Mw3B6b2k4gNc130_provenance.