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- NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_assertion type Assertion NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_head.
- NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_assertion wasGeneratedBy ECO_0000203 NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_provenance.
- NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_assertion wasDerivedFrom befree-20140225 NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_provenance.
- NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_assertion SIO_000772 22271696 NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_provenance.
- NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_assertion evidence source_evidence_literature NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_provenance.
- NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_assertion description "[Mevalonic aciduria (MA) represents the severest form of mevalonate kinase deficiency due to recessively inherited, loss-of-function MVK mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777303.RAeNJBNpOTyYms2AVKPBhKqaVGyubQ1AhfqGupq7SZkV8130_provenance.