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- source_evidence_literature type ECO_0000212 NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_provenance.
- NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_assertion description "[On the basis of the structural analysis, this study further demonstrated that the p.R225Q mutation abolished DNA binding by RUNX2 and its results also suggested that other genetic and/or environmental factors could affect the CCD phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_provenance.
- NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_assertion evidence source_evidence_literature NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_provenance.
- NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_assertion SIO_000772 24634175 NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_provenance.
- NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_assertion wasDerivedFrom befree-20150227 NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_provenance.
- NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_assertion wasGeneratedBy ECO_0000203 NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP284789.RAl5I9bz7iuWHaB1ooLzhSTLWKmXzZnWDSO5tWh1SVjsI130_provenance.