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- source_evidence_literature type ECO_0000212 NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_provenance.
- NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_assertion description "[Mutations in the kidney isozyme of human 11-hydroxysteroid dehydrogenase (11-HSD2) cause apparent mineralocorticoid excess, an autosomal recessive form of familial hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_provenance.
- NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_assertion evidence source_evidence_literature NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_provenance.
- NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_assertion SIO_000772 10523339 NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_provenance.
- NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_assertion wasDerivedFrom befree-20140225 NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_provenance.
- NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_assertion wasGeneratedBy ECO_0000203 NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP505845.RAVYsQuzgOkwxN9LpTsJsc1BHWEQjsSOjNV5aEOhTrREw130_provenance.