Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_provenance.
- befree-2016 importedOn "2016-02-19" NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_provenance.
- NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_assertion wasGeneratedBy ECO_0000203 NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_provenance.
- NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_assertion wasDerivedFrom befree-2016 NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_provenance.
- NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_assertion SIO_000772 10699051 NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_provenance.
- NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_assertion evidence source_evidence_literature NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_provenance.
- NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_assertion description "[We have previously shown that disruption of the human CREB binding protein (CREBBP or CBP) gene, either by these gross chromosomal rearrangements or by point mutations, leads to RTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276823.RAGH0AQM7BVEGh5uo2WI62FTW1MrxQ0SJfZ4vvU6vGmeE130_provenance.