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- source_evidence_literature type ECO_0000212 NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_provenance.
- NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_assertion description "[These results suggest that CACNA1C may be associated with secondary hyperparathyroidism. In addition, the haplotype-based approach may be useful to screen for key molecules associated with complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_provenance.
- NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_assertion evidence source_evidence_literature NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_provenance.
- NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_assertion SIO_000772 20424473 NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_provenance.
- NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_assertion wasDerivedFrom gad-20150221 NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_provenance.
- NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_assertion wasGeneratedBy ECO_0000203 NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_provenance.
- gad-20150221 importedOn "2015-02-21" NP133212.RAvbINhqhAynM1IFijYZi_4FzLRs76ZbAajor3PHja_ew130_provenance.