Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_provenance.
- NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_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." NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_provenance.
- NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_assertion evidence source_evidence_literature NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_provenance.
- NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_assertion SIO_000772 20591826 NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_provenance.
- NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_assertion wasDerivedFrom befree-2016 NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_provenance.
- NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_assertion wasGeneratedBy ECO_0000203 NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_provenance.
- befree-2016 importedOn "2016-02-19" NP822624.RAeMNLZ_8tVUe3fsKPAQxpT3jVCKHrKijC64sI1DAS1Q0130_provenance.