Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_provenance.
- NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_assertion description "[Within HD subtypes, expression of IP-10 and Mig was highest in the mixed cellularity (MC) subtype, whereas expression of eotaxin and MDC was highest in the nodular sclerosis (NS) subtype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_provenance.
- NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_assertion evidence source_evidence_literature NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_provenance.
- NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_assertion SIO_000772 10194423 NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_provenance.
- NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_assertion wasDerivedFrom befree-20140225 NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_provenance.
- NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_assertion wasGeneratedBy ECO_0000203 NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP304149.RA12uUrbQfvFur7xZtbcSY3JULMUiplk2L63V-gWJ_3YY130_provenance.