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- source_evidence_literature type ECO_0000212 NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_provenance.
- NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_assertion description "[The consistent identification by RT-PCR of the fusion of the PML and RAR alpha genes in AML3 patients suggest that this method will provide a useful tool for the diagnosis and detection of minimal residual disease in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_provenance.
- NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_assertion evidence source_evidence_literature NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_provenance.
- NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_assertion SIO_000772 1375840 NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_provenance.
- NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_assertion wasDerivedFrom befree-20150227 NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_provenance.
- NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_assertion wasGeneratedBy ECO_0000203 NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_provenance.
- befree-20150227 importedOn "2015-02-27" NP665612.RARYOVfJ-iIxNbuOXsy1V6itVbiCrV_k5QSijk_whsNik130_provenance.