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- NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_assertion type Assertion NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_head.
- NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_assertion description "[The frequency of UBQLN2 and PFN1 genetic variants in the FTLD patients was low at 0.30% and 0.91% respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_provenance.
- NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_assertion evidence source_evidence_literature NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_provenance.
- NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_assertion SIO_000772 23312802 NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_provenance.
- NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_assertion wasDerivedFrom befree-20150227 NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_provenance.
- NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_assertion wasGeneratedBy ECO_0000203 NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_provenance.