Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_provenance.
- NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_assertion description "[These results demonstrate that SAP defects are rarely observed in CVID patients. We suggest that routine screening of SAP may only be necessary in patients with other suggestive clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_provenance.
- NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_assertion evidence source_evidence_literature NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_provenance.
- NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_assertion SIO_000772 15320910 NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_provenance.
- NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_assertion wasDerivedFrom gad-20150221 NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_provenance.
- NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_assertion wasGeneratedBy ECO_0000203 NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP87446.RAtlv16GlBuVWnKqthDNHJKQnn6jCN0_JTqHhovFzqVqg130_provenance.