Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_assertion> ?p ?o ?g. }
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- NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_assertion type Assertion NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_head.
- NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_assertion description "[Huntington disease is a neurodegenerative disorder caused by a CAG repeat amplification in the gene huntingtin (HTT) that is reflected by a polyglutamine expansion in the Htt protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_provenance.
- NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_assertion evidence source_evidence_literature NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_provenance.
- NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_assertion SIO_000772 22556411 NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_provenance.
- NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_assertion wasDerivedFrom befree-2016 NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_provenance.
- NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_assertion wasGeneratedBy ECO_0000203 NP979624.RArRI-meM9tPUEKTqbgVF-eWnpwNHWPa8zq_-Yx0WUND4130_provenance.