Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_provenance.
- NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_assertion description "[Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_provenance.
- NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_assertion evidence source_evidence_literature NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_provenance.
- NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_assertion SIO_000772 9539740 NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_provenance.
- NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_assertion wasDerivedFrom befree-20150227 NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_provenance.
- NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_assertion wasGeneratedBy ECO_0000203 NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_provenance.