Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_provenance.
- NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_assertion description "[We conclude that variant MBL2 structural genotype constitutes a significant risk factor for reactive amyloidosis in RA and that the increased risk is probably related to MBL-mediated impairment of mononuclear phagocyte function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_provenance.
- NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_assertion evidence source_evidence_literature NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_provenance.
- NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_assertion SIO_000772 17875183 NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_provenance.
- NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_assertion wasDerivedFrom gad-20150221 NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_provenance.
- NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_assertion wasGeneratedBy ECO_0000203 NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP111894.RA0qO2_4ds6CHhN3ICvPbMRz3hKGKomBhfb1ck9eb4wXg130_provenance.