Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_provenance.
- NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_assertion description "[The results support the concept that deletions as well as depletion of mtDNA are involved in the pathogenesis of Alpers-Huttenlocher syndrome and add 3 new POLG1 mutations associated with an early-onset neurodegenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_provenance.
- NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_assertion evidence source_evidence_literature NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_provenance.
- NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_assertion SIO_000772 16896309 NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_provenance.
- NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_assertion wasDerivedFrom befree-20140225 NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_provenance.
- NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_assertion wasGeneratedBy ECO_0000203 NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP584681.RAzGT-tFF4EFjWZSPLxY4yRdK5Ja64zqaX1wGyNX1ScnY130_provenance.