Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP185567.RAsGAFmU3Rvd19EieCuidbhXnHACBIvhKTfwTx5Dg1Z-Q130_provenance.