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- source_evidence_literature type ECO_0000212 NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_provenance.
- NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_assertion wasGeneratedBy ECO_0000203 NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_provenance.
- NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_assertion wasDerivedFrom befree-20150227 NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_provenance.
- NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_assertion SIO_000772 15643505 NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_provenance.
- NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_assertion evidence source_evidence_literature NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_provenance.
- NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_assertion description "[Although the frequency of MSI (25%) or a loss of hMLH1 and/or hMSH2 expression (23%) was relatively low in STS cases, a loss of hMLH1 and/or hMSH2 was recognized in 5 out of 10 MSI-positive cases (50%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569965.RADrXDNDO_LDTP7tast4rxMTFZum_7FAy4fonwLcJJ5K8130_provenance.