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- source_evidence_literature type ECO_0000212 NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_provenance.
- NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_assertion description "[The clinical manifestation of MJD is dependent on the presence of an expansion of the (CAG)(n) motif within exon 10 of the ATXN3 gene, located at 14q32.1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_provenance.
- NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_assertion evidence source_evidence_literature NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_provenance.
- NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_assertion SIO_000772 19935829 NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_provenance.
- NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_assertion wasDerivedFrom befree-2016 NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_provenance.
- NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_assertion wasGeneratedBy ECO_0000203 NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_provenance.
- befree-2016 importedOn "2016-02-19" NP777619.RA1BSo3EPXE0fTYlDr3vbmluetZIlIr-UarvuH4IOKUT0130_provenance.