Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_provenance.
- NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_assertion wasGeneratedBy ECO_0000203 NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_provenance.
- NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_assertion wasDerivedFrom befree-2016 NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_provenance.
- NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_assertion SIO_000772 19533794 NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_provenance.
- NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_assertion evidence source_evidence_literature NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_provenance.
- NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_assertion description "[Mutations in CREBBP and EP300 were identified in approximately 50% and 3% of RSTS patients, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745793.RAm0FhW6lyDTrABeNLejT75xZwqGKZH7FS4iXUHvS0ysQ130_provenance.