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- NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_assertion type Assertion NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_head.
- NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_assertion description "[Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.
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- NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_assertion SIO_000772 19221116 NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.
- NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_assertion wasDerivedFrom gad-20150221 NP118872.RANh2eOrrzCCIdVmWrRWFyXHvL4FJvyhlqosdRon9XAWw130_provenance.
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