Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_provenance.
- NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_assertion description "[In this study, a mutation in vasopressin Type 2 receptor (V2R) in a patient with hereditary nephrogenic diabetes insipidus (NDI) has been identified and characterized.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_provenance.
- NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_assertion evidence source_evidence_literature NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_provenance.
- NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_assertion SIO_000772 8704106 NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_provenance.
- NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_assertion wasDerivedFrom befree-20140225 NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_provenance.
- NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_assertion wasGeneratedBy ECO_0000203 NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP223469.RATlzKYINPDAcfpgb9BzmicHTV4bv0xtXoJ_l5-KZHqh8130_provenance.