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- source_evidence_literature type ECO_0000212 NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_provenance.
- NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_assertion description "[Mutations in AQP2 cause autosomal nephrogenic diabetes insipidus (NDI), a disease that renders the kidney unresponsive to vasopressin, resulting in polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_provenance.
- NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_assertion evidence source_evidence_literature NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_provenance.
- NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_assertion SIO_000772 19701945 NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_provenance.
- NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_assertion wasDerivedFrom befree-20150227 NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_provenance.
- NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_assertion wasGeneratedBy ECO_0000203 NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP249349.RAEA1KfMIhKdgNK7PLRuhrVw2YoFN0PCQcHlqj1IKyQC0130_provenance.