Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_assertion> ?p ?o ?g. }
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- NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_assertion type Assertion NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_head.
- NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_assertion description "[Microdeletions of movement disorder genes including epsilon-sarcoglycan (SGCE) and thyroid transcription factor-1 (TITF1) have been described in patients with myoclonus dystonia and benign hereditary chorea respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_provenance.
- NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_assertion evidence source_evidence_literature NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_provenance.
- NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_assertion SIO_000772 22515636 NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_provenance.
- NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_assertion wasDerivedFrom befree-2016 NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_provenance.
- NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_assertion wasGeneratedBy ECO_0000203 NP976012.RAL1r-Qw6AWHQL1K5XUgHMfzPq5tABJ08i9iSNfGV3rdU130_provenance.