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- source_evidence_literature type ECO_0000212 NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_provenance.
- NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_provenance.
- NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_assertion evidence source_evidence_literature NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_provenance.
- NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_assertion SIO_000772 9247735 NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_provenance.
- NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_assertion wasDerivedFrom befree-20150227 NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_provenance.
- NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_assertion wasGeneratedBy ECO_0000203 NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP669969.RAa50StxAIIIloveEYi1gXFVGnw4AWKGkxoEH4bnyWdi8130_provenance.