Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_provenance.
- NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_assertion description "[In both Group A and Group AGM, more patients carrying the variant allele had episodes of upper respiratory or gastrointestinal infections prior to onset or exacerbation of IgAN than wild homozygotes (GGC/GGC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_provenance.
- NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_assertion evidence source_evidence_literature NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_provenance.
- NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_assertion SIO_000772 11487077 NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_provenance.
- NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_assertion wasDerivedFrom befree-20150227 NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_provenance.
- NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_assertion wasGeneratedBy ECO_0000203 NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP485747.RAc752WzzVFyb1ufGrdHfgYNT-c0u3-VcRPfTXk0VOmGQ130_provenance.