Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_provenance.
- NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_assertion description "[To facilitate a rapid and practical molecular diagnosis of 21-hydroxylase deficiency (21-OHD), we developed a polymerase chain reaction (PCR) test in which only the 21-OH gene (CYP21) is amplified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_provenance.
- NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_assertion evidence source_evidence_literature NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_provenance.
- NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_assertion SIO_000772 10982478 NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_provenance.
- NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_assertion wasDerivedFrom befree-2016 NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_provenance.
- NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_assertion wasGeneratedBy ECO_0000203 NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_provenance.
- befree-2016 importedOn "2016-02-19" NP294793.RAr7E2u3sPRwoRCixiJ__jbCpUNmFaVy7IRf3GWooRc8I130_provenance.