Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_provenance.
- NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_assertion description "[Most cases of congenital adrenal hyperplasia (CAH) are caused by mutations in this gene, and most mutations appear to arise from gene conversion-like events involving the transfer of deleterious sequences from the pseudogene, CYP21P, which is located within 30 kb of CYP21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_provenance.
- NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_assertion evidence source_evidence_literature NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_provenance.
- NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_assertion SIO_000772 9836705 NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_provenance.
- NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_assertion wasDerivedFrom befree-2016 NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_provenance.
- NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_assertion wasGeneratedBy ECO_0000203 NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_provenance.
- befree-2016 importedOn "2016-02-19" NP1410071.RAVtV4Mk2AuqRD-YZQSQhR7USIKxz7-iVfk1FVDs5Dxec130_provenance.