Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_provenance.
- NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_assertion wasGeneratedBy ECO_0000203 NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_provenance.
- NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_assertion wasDerivedFrom befree-20140225 NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_provenance.
- NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_assertion SIO_000772 22894767 NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_provenance.
- NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_assertion evidence source_evidence_literature NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_provenance.
- NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_assertion description "[Zellweger syndrome (ZS) is a peroxisome biogenesis disorder due to mutations in any one of 13 PEX genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP673910.RAmCB4Fz9KsZEF2mIoQ-O_4LxprYlpbteVFlq-4tZ1nOY130_provenance.