Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_provenance.
- NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_assertion wasGeneratedBy ECO_0000203 NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_provenance.
- NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_assertion wasDerivedFrom befree-20150227 NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_provenance.
- NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_assertion SIO_000772 11562939 NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_provenance.
- NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_assertion evidence source_evidence_literature NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_provenance.
- NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_assertion description "[The search for targets of FMRP (the product of FMR1, the mutated gene in Fragile X syndrome) has predominantly focused on identifying transcripts that are regulated by this RNA-binding protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887918.RAtu6R-oSILFtZni_H6idJt6R5PnRQDEaKIPfw0YQULrY130_provenance.