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- source_evidence_literature type ECO_0000212 NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance.
- NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_assertion description "[Although p14 inactivation or overexpression of the human murine double minute homolog (HDM2) were frequent in LMS and UPS and could substitute for TP53 mutation or deletion, such alterations were rare in angiosarcomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance.
- NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_assertion evidence source_evidence_literature NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance.
- NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_assertion SIO_000772 22648906 NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance.
- NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_assertion wasDerivedFrom befree-2016 NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance.
- NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_assertion wasGeneratedBy ECO_0000203 NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance.
- befree-2016 importedOn "2016-02-19" NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance.