Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_provenance.
- NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_assertion description "[In contrast, the Hp allele frequencies of the SLE patients were 0.733 (Hp(2)), 0.233 (Hp(1S)), and 0.033 (Hp1(1F)), which clearly indicated an increased frequency of Hp(2), a similar proportion of Hp(1S) and a diminished proportion of Hp(1F) in SLE patients compared with that in healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_provenance.
- NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_assertion evidence source_evidence_literature NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_provenance.
- NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_assertion SIO_000772 16544281 NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_provenance.
- NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_assertion wasDerivedFrom befree-20140225 NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_provenance.
- NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_assertion wasGeneratedBy ECO_0000203 NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_provenance.
- befree-20140225 importedOn "2014-02-25" NP661430.RAFozdQfnkJfJEonIsmyHnNN8CV2tVzTUJdAY3I3GQ0Ak130_provenance.