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- NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_assertion type Assertion NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_head.
- NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_assertion description "[The X-linked dominant form of Charcot-Marie-Tooth disease (CMTX) is associated with mutations in a gene coding for the gap-junction protein connexin 32 (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_provenance.
- NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_assertion evidence source_evidence_literature NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_provenance.
- NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_assertion SIO_000772 9272161 NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_provenance.
- NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_assertion wasDerivedFrom befree-2016 NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_provenance.
- NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_assertion wasGeneratedBy ECO_0000203 NP1379471.RAalEVRdf5tWoxugWv8LhjOUSuJ4xdkXRnOT0wqUG2xdo130_provenance.