Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_provenance.
- NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_assertion description "[Context: Steroid 21-hydroxylase deficiency is the most common enzymatic defect causing congenital adrenal hyperplasia with genotype/phenotype relationships for common mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_provenance.
- NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_assertion evidence source_evidence_literature NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_provenance.
- NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_assertion SIO_000772 20080860 NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_provenance.
- NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_assertion wasDerivedFrom gad-20150221 NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_provenance.
- NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_assertion wasGeneratedBy ECO_0000203 NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_provenance.
- gad-20150221 importedOn "2015-02-21" NP162724.RA8-ksMXw1uICcvJ4n7v-kpOhkbPoc4Yon02HJJTxnA4A130_provenance.