Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_provenance.
- NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_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." NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_provenance.
- NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_assertion evidence source_evidence_literature NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_provenance.
- NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_assertion SIO_000772 3018042 NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_provenance.
- NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_assertion wasDerivedFrom befree-20140225 NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_provenance.
- NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_assertion wasGeneratedBy ECO_0000203 NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP481769.RAwcg8FKRWc0--NskGVbGtFp8E2xUMKXEkxZN9glfbJTU130_provenance.