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- source_evidence_literature type ECO_0000212 NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_provenance.
- befree-2016 importedOn "2016-02-19" NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_provenance.
- NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_assertion wasGeneratedBy ECO_0000203 NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_provenance.
- NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_assertion wasDerivedFrom befree-2016 NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_provenance.
- NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_assertion SIO_000772 16728546 NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_provenance.
- NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_assertion evidence source_evidence_literature NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_provenance.
- NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_assertion description "[Congenital adrenal hyperplasia (CAH) shows a range of severity which is explained in part by the different mutations of the CYP21 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551610.RAClGF-omNFSVdteT4KSeWMw03aTr7yBFgCOIbZpsewfM130_provenance.