Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_provenance.
- NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_assertion description "[CGD is a rare inherited immunodeficiency syndrome, caused by the phagocytes' inability to produce (sufficient) reactive oxygen metabolites.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_provenance.
- NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_assertion evidence source_evidence_literature NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_provenance.
- NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_assertion SIO_000772 9618766 NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_provenance.
- NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_assertion wasDerivedFrom befree-20150227 NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_provenance.
- NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_assertion wasGeneratedBy ECO_0000203 NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP338893.RARxSzOsGp1uNkrLowmGZMpoERha_buYJ5tnPx2B6KwPQ130_provenance.