Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_assertion> ?p ?o ?g. }
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- NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_assertion type Assertion NP985416.RAMJgmj2Q8LjRH0ucZ6y_EV8hYOSvKwoaM7pQHYp4C-GE130_head.
- 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.