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- source_evidence_literature type ECO_0000212 NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_provenance.
- NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_assertion description "[Two novel mutations were identified in each of AVPR2 and AQP2 underlying Congenital Nephrogenic Diabetes Insipidus in Arab families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_provenance.
- NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_assertion evidence source_evidence_literature NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_provenance.
- NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_assertion SIO_000772 16845277 NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_provenance.
- NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_assertion wasDerivedFrom lhgdn-20090331 NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_provenance.
- NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_assertion wasGeneratedBy ECO_0000203 NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP218445.RA5ssNTu93bBrmYusc5bqer9x0le0y0Qyx8FwFPoukkEQ130_provenance.