Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_provenance.
- NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_assertion description "[Thus, attenuation of MCP-1 upregulation by inhibiting ERK phosphorylation might be a promising approach to treat CMT1X and other so far untreatable inherited peripheral neuropathies in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_provenance.
- NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_assertion evidence source_evidence_literature NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_provenance.
- NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_assertion SIO_000772 20591826 NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_provenance.
- NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_assertion wasDerivedFrom befree-20140225 NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_provenance.
- NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_assertion wasGeneratedBy ECO_0000203 NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP780928.RAY4NsdC4QnZ5L8B7vkct722BkwE3czHU0V8CaWAMr8FQ130_provenance.