Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_provenance.
- NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_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." NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_provenance.
- NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_assertion evidence source_evidence_literature NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_provenance.
- NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_assertion SIO_000772 9539740 NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_provenance.
- NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_assertion wasDerivedFrom befree-20150227 NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_provenance.
- NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_assertion wasGeneratedBy ECO_0000203 NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP616251.RAI8hrP9q8NJfwb-03AsW29t3RoAm0OkckUNZJ3MdBbQQ130_provenance.