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- source_evidence_literature type ECO_0000212 NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_provenance.
- NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_assertion wasGeneratedBy ECO_0000203 NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_provenance.
- NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_assertion wasDerivedFrom befree-20140225 NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_provenance.
- NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_assertion SIO_000772 15921863 NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_provenance.
- NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_assertion evidence source_evidence_literature NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_provenance.
- NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_assertion description "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP785436.RAMq_c8DkrndiSy1Dk0VDfQ943-9zx8wYZrDEvkw6D0hE130_provenance.