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- source_evidence_literature type ECO_0000212 NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_provenance.
- NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_assertion description "[The identification, characterization, and mutational analysis of three different genes, namely the prepro-arginine-vasopressin-neurophysin II gene (prepro-AVP-NPII), the arginine-vasopressin receptor 2 gene (AVPR2), and the vasopressin-sensitive water channel gene (aquaporin-2, AQP2), provide the basis for our understanding of three different hereditary forms of diabetes insipidus: autosomal dominant neurogenic diabetes insipidus, X-linked nephrogenic diabetes insipidus, and autosomal recessive nephrogenic diabetes insipidus, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_provenance.
- NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_assertion evidence source_evidence_literature NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_provenance.
- NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_assertion SIO_000772 7541187 NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_provenance.
- NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_assertion wasDerivedFrom befree-20150227 NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_provenance.
- NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_assertion wasGeneratedBy ECO_0000203 NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP258151.RALQ_LVAwCDsiaRWTWGJnWycR5i_p5qsewzWHds8jGdUo130_provenance.