Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_assertion> ?p ?o ?g. }
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- NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_assertion type Assertion NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_head.
- NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_assertion description "[The growing list ofneurodegenerative and neuromuscular diseases caused by dynamic mutations includes Huntington's disease (HD), spinobulbar muscular atrophy (SBMA), dentatorubral-pallidoluysian atrophy (DRPLA), a number of spinocerebellar ataxias (SCAs), oculopharyngeal muscular dystrophy (OPMD), myotonic dystrophy Type 1 and 2 (DM1 and 2), Huntington's disease-like 2 (HDL-2), Friedrich's ataxia (FRDA), Fragile X associated tremor ataxia syndrome (FXTAS), Fragile XE (FRAXE) and Fragile XA (FRAXA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_provenance.
- NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_assertion evidence source_evidence_literature NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_provenance.
- NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_assertion SIO_000772 23560305 NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_provenance.
- NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_assertion wasDerivedFrom befree-20150227 NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_provenance.
- NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_assertion wasGeneratedBy ECO_0000203 NP929532.RA3o-ZqdenU8UDreTrWN6hZ7MNLza1lOaq6OZvJK5GOXs130_provenance.