Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_assertion> ?p ?o ?g. }
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- NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_assertion type Assertion NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_head.
- NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_assertion description "[Huntington disease (HD) is an inherited neurological disorder caused by a polyglutamine expansion in the protein huntingtin and is characterized by selective neurodegeneration that preferentially occurs in striatal medium spiny neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_provenance.
- NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_assertion evidence source_evidence_literature NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_provenance.
- NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_assertion SIO_000772 20018729 NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_provenance.
- NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_assertion wasDerivedFrom befree-2016 NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_provenance.
- NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_assertion wasGeneratedBy ECO_0000203 NP782175.RAAeOnKPUs-1B-fFcZCjLyR1PXsk5Ixkfq1zNa_j3RPeU130_provenance.