Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_assertion> ?p ?o ?g. }
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- NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_assertion type Assertion NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_head.
- NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_assertion description "[Congenital myotonic dystrophy (CDM1) and myotonic dystrophy of type 1 (DM1) or of type 2 (DM2) are caused by the expression of mutant RNAs containing expanded CUG or CCUG repeats, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_provenance.
- NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_assertion evidence source_evidence_literature NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_provenance.
- NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_assertion SIO_000772 21623381 NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_provenance.
- NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_assertion wasDerivedFrom befree-20140225 NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_provenance.
- NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_assertion wasGeneratedBy ECO_0000203 NP457472.RAhFMb1EAkbU7OewgdUx01JfxtwVu-tGOLkgRPiFzSmng130_provenance.