Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_provenance.
- NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_assertion description "[BACH1 was significantly overexpressed in fetal DS (p < 0.008) as compared to controls whereas RUNX1 and ERG proteins were comparable between groups, and SIM2 l was not detectable in any specimen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_provenance.
- NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_assertion evidence source_evidence_literature NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_provenance.
- NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_assertion SIO_000772 15068251 NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_provenance.
- NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_assertion wasDerivedFrom befree-20150227 NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_provenance.
- NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_assertion wasGeneratedBy ECO_0000203 NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP521767.RACZGu35Bp4XbJ8VP5-hR16BQweklid9T_MwC6drIgv_c130_provenance.