Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion type Assertion NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_head.
- NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion description "[The mutation causing myotonic dystrophy (DM) has recently been identified as an unstable CTG trinucleotide repeat located in the 3' untranslated region of a gene encoding for a protein with putative serine-threonine protein kinase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion evidence source_evidence_literature NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion SIO_000772 8499920 NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion wasDerivedFrom befree-20140225 NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.
- NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_assertion wasGeneratedBy ECO_0000203 NP570335.RAET2AzAky5H6pB4hX_yzLq1a3LjvwyykoZqnDV1GCCSk130_provenance.