Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_provenance.
- NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_assertion description "[Several autoimmune disorders as well as congenital adrenal hyperplasia (CAH) are either associated or closely linked with genetic variants of the fourth component of complement (C4A and C4B) and the enzyme steroid 21-hydroxylase (21-OH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_provenance.
- NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_assertion evidence source_evidence_literature NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_provenance.
- NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_assertion SIO_000772 3018042 NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_provenance.
- NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_assertion wasDerivedFrom befree-20140225 NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_provenance.
- NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_assertion wasGeneratedBy ECO_0000203 NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP807516.RAGoktaP8wqPNleWl2F3O_wAhBw0seMLMVfr99jBmrE1k130_provenance.