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- source_evidence_literature type ECO_0000212 NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_provenance.
- NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_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." NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_provenance.
- NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_assertion evidence source_evidence_literature NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_provenance.
- NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_assertion SIO_000772 20424473 NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_provenance.
- NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_assertion wasDerivedFrom gad-20150221 NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_provenance.
- NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_assertion wasGeneratedBy ECO_0000203 NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP173797.RA2b53nGw-utwxbMOaNBp1YwLz5t4tAhZhH3-171hKVRQ130_provenance.