Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_assertion type Assertion NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_head.
- NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_assertion description "[We extended the search for mutations to the EP300 gene and showed that mutations in EP300 also cause this disorder/are the first mutations identified in EP300 for a congenital disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_provenance.
- NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_assertion evidence source_evidence_literature NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_provenance.
- NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_assertion SIO_000772 15706485 NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_provenance.
- NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_assertion wasDerivedFrom lhgdn-20090331 NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_provenance.
- NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_assertion wasGeneratedBy ECO_0000203 NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_provenance.