Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion description "[Neonatal screening for steroid 21-hydroxylase (CYP21) deficiency is performed to identify congenital adrenal hyperplasia (CAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion evidence source_evidence_literature NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion SIO_000772 15608154 NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion wasDerivedFrom befree-2016 NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion wasGeneratedBy ECO_0000203 NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- befree-2016 importedOn "2016-02-19" NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.