Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_provenance.
- 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.
- uniprot-20130724 importedOn "2013-07-24" NP4882.RAQIt-oWe5gITmGQI1jVLvfB7MBzyqGzTWTp-xC_JbCfs130_provenance.