Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_provenance.
- NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_assertion description "[A rare variant of the C4B locus, C4B*2.9, was found in 25% of these patients compared with only 2% of the normal population--a relative risk of 22.1 for glomerulonephritis in individuals with this variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_provenance.
- NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_assertion evidence source_evidence_literature NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_provenance.
- NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_assertion SIO_000772 6143186 NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_provenance.
- NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_assertion wasDerivedFrom befree-20140225 NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_provenance.
- NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_assertion wasGeneratedBy ECO_0000203 NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477496.RAWyIGUxgHT1bFaCoXMCxszSUK2r1UEfBuEddIXQHdvcg130_provenance.