Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_provenance.
- NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_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." NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_provenance.
- NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_assertion evidence source_evidence_literature NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_provenance.
- NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_assertion SIO_000772 9618766 NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_provenance.
- NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_assertion wasDerivedFrom befree-2016 NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_provenance.
- NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_assertion wasGeneratedBy ECO_0000203 NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1396891.RAJ9jNO45RjIDFTSqKVGzpg4cfM7kRf4lLKnMm3jZxEzs130_provenance.