Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_provenance.
- NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_assertion description "[Similarly, skeletal muscle weakness, increased Nox4 binding to RyR1 and oxidation of RyR1 were present in a mouse model of Camurati-Engelmann disease, a nonmalignant metabolic bone disorder associated with increased TGF-? activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_provenance.
- NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_assertion evidence source_evidence_literature NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_provenance.
- NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_assertion SIO_000772 26457758 NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_provenance.
- NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_assertion wasDerivedFrom befree-2016 NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_provenance.
- NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_assertion wasGeneratedBy ECO_0000203 NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_provenance.
- befree-2016 importedOn "2016-02-19" NP1294848.RAtxCKo7qLFz0I5gsHT60bVQEvkVnW9RQpnvOYdUTJW4g130_provenance.