Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_assertion type Assertion NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_head.
- NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_assertion description "[This is the first genetic study of Rett syndrome in New Zealand patients describing the MECP2 mutational spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_provenance.
- NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_assertion evidence source_evidence_literature NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_provenance.
- NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_assertion SIO_000772 19652677 NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_provenance.
- NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_assertion wasDerivedFrom befree-2016 NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_provenance.
- NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_assertion wasGeneratedBy ECO_0000203 NP755276.RADuQ6UDy5geNihWtvJMzwYC9rJMu_9Hub_h6sq4ypx80130_provenance.