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- source_evidence_literature type ECO_0000212 NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_provenance.
- NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_assertion description "[The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_provenance.
- NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_assertion evidence source_evidence_literature NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_provenance.
- NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_assertion SIO_000772 18411254 NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_provenance.
- NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_assertion wasDerivedFrom befree-2016 NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_provenance.
- NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_assertion wasGeneratedBy ECO_0000203 NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_provenance.
- befree-2016 importedOn "2016-02-19" NP665729.RAsVPDxrcAOZOP-L9SrzPIqUCLkgwfBkJUeZiZE8AMmMk130_provenance.