Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_assertion type Assertion NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_head.
- NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_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." NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_provenance.
- NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_assertion evidence source_evidence_curated NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_provenance.
- NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_assertion SIO_000772 9539740 NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_provenance.
- NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_assertion wasDerivedFrom uniprot-20130724 NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_provenance.
- NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_assertion wasGeneratedBy ECO_0000218 NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_provenance.