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- source_evidence_literature type ECO_0000212 NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_provenance.
- NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_provenance.
- NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_assertion evidence source_evidence_literature NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_provenance.
- NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_assertion SIO_000772 18723471 NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_provenance.
- NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_assertion wasDerivedFrom gad-20150221 NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_provenance.
- NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_assertion wasGeneratedBy ECO_0000203 NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_provenance.