Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_provenance.
- NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_assertion description "[The aim of this study was to explore whether the FCRL3 -169 C/T polymorphism confers susceptibility to RA and SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_provenance.
- NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_assertion evidence source_evidence_literature NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_provenance.
- NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_assertion SIO_000772 19690864 NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_provenance.
- NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_assertion wasDerivedFrom befree-20140225 NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_provenance.
- NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_assertion wasGeneratedBy ECO_0000203 NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717696.RAlbS00-NRdlyzAWt2UPu8pEAQbn53zFgW5aP7GxFpzJg130_provenance.