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- NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_assertion type Assertion NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_head.
- NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_assertion description "[FMR1 is an RNA-binding protein that is either absent or mutated in patients affected by the fragile X syndrome, the most common inherited cause of mental retardation in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_provenance.
- NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_assertion evidence source_evidence_literature NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_provenance.
- NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_assertion SIO_000772 10496225 NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_provenance.
- NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_assertion wasDerivedFrom befree-20140225 NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_provenance.
- NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_assertion wasGeneratedBy ECO_0000203 NP236650.RA_CqJAPV_6-hXo0tff8YFfDDVCz4yL96pWDfKJG7HEuQ130_provenance.