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- NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_assertion type Assertion NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_head.
- 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.
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- 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.