Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP895445.RA1-lgpXoyMFGY7yDfW7mejsQCqRSRvd8awaCCWeovXVU130_provenance.