Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_assertion> ?p ?o ?g. }
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- NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_assertion type Assertion NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_head.
- NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_assertion wasGeneratedBy ECO_0000203 NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_provenance.
- NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_assertion wasDerivedFrom befree-20150227 NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_provenance.
- NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_assertion SIO_000772 14506070 NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_provenance.
- NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_assertion evidence source_evidence_literature NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_provenance.
- NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_assertion description "[The frequency of chorea at onset suggests that this diagnosis should also be considered in children with chorea who do not carry the IT15 mutation responsible for Huntington's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445304.RAWKKauf30DOIGGBtICaQXF7PvN34LAq0vKnf01UkDt9M130_provenance.