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- source_evidence_literature type ECO_0000212 NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_provenance.
- NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_provenance.
- NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_assertion evidence source_evidence_literature NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_provenance.
- NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_assertion SIO_000772 15110905 NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_provenance.
- NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_assertion wasDerivedFrom befree-20150227 NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_provenance.
- NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_assertion wasGeneratedBy ECO_0000203 NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_provenance.