Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_provenance.
- befree-2016 importedOn "2016-02-19" NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_provenance.
- NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_assertion wasGeneratedBy ECO_0000203 NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_provenance.
- NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_assertion wasDerivedFrom befree-2016 NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_provenance.
- NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_assertion SIO_000772 22407275 NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_provenance.
- NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_assertion evidence source_evidence_literature NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_provenance.
- NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966877.RADLL0OwBx0CMP0DjxuImztd0GUwefp6we5SKgQtU3k-E130_provenance.