Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP209215.RAVT7g-UnF-jT-1ZpRtiol9gRyEGbsH6dVQDaMDxggtA4130_provenance.