Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_provenance.
- NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_assertion description "[IFN-?-1b induces NCOA7-AS (alternative start) expression in peripheral blood mononuclear cells (PBMCs) obtained from healthy individuals and multiple sclerosis patients and human fetal brain cells, astrocytoma, neuroblastoma, and fibrosarcoma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_provenance.
- NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_assertion evidence source_evidence_literature NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_provenance.
- NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_assertion SIO_000772 25330068 NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_provenance.
- NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_assertion wasDerivedFrom befree-2016 NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_provenance.
- NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_assertion wasGeneratedBy ECO_0000203 NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1230768.RAC3rQswWn6tOqMUCyowJehzt_OWQDnnokilw1F-Lcx6k130_provenance.