Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_assertion> ?p ?o ?g. }
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- NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_assertion type Assertion NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_head.
- NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_assertion description "[Huntington disease (HD) is a neurodegenerative disorder caused by a CAG repeat expansion in the HD gene resulting in expression of an uninterrupted polyglutamine stretch within the N-terminus of its protein product huntingtin (htt).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_provenance.
- NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_assertion evidence source_evidence_literature NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_provenance.
- NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_assertion SIO_000772 10716661 NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_provenance.
- NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_assertion wasDerivedFrom befree-2016 NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_provenance.
- NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_assertion wasGeneratedBy ECO_0000203 NP277973.RAtxv7sf9EM7nQAUWMI-QRrCFCIx7nQv8GX0MBu80UGTg130_provenance.