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- source_evidence_literature type ECO_0000212 NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_provenance.
- NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_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." NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_provenance.
- NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_assertion evidence source_evidence_literature NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_provenance.
- NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_assertion SIO_000772 14581671 NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_provenance.
- NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_assertion wasDerivedFrom befree-20140225 NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_provenance.
- NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_assertion wasGeneratedBy ECO_0000203 NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP505453.RAvauzjizK46EfL1Eo6DfLM6RfEnG0cKMrDStXmg8YuZY130_provenance.