Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_assertion> ?p ?o ?g. }
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- NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_assertion type Assertion NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_head.
- NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_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." NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_provenance.
- NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_assertion evidence source_evidence_literature NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_provenance.
- NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_assertion SIO_000772 15706485 NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_provenance.
- NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_assertion wasDerivedFrom lhgdn-20090331 NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_provenance.
- NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_assertion wasGeneratedBy ECO_0000203 NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_provenance.